The World Health Organization plans to eradicate sleeping sickness by the year 2030. [37] [38] Trypanosoma brucei gambiense [39] 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 Angola 1498 2094 2406 1796 1274 2441 6726 8275 6610 5351 4546 4577 3621 3115 2280 1727 1105 648 517 247 211 154 70 69 36 35 19 18 79 30 Benin 0 0 2 1 0 0 0 0 0 20 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 Burkina Faso 27 27 20 17 18 13 12 1 15 15 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 0 Cameroon 86 69 21 3 20 21 17 10 54 32 27 14 32 33 17 3 15 7 13 24 16 15 7 6 7 6 6 5 7 17 Central African Republic 308 197 362 262 368 676 492 730 1068 869 988 718 572 539 738 666 460 654 1194 1054 395 132 381 59 194 147 124 76 57 86 Chad 20 221 149 65 214 315 178 122 134 187 153 138 715 222 483 190 276 97 196 510 232 276 197 195 95 67 53 28 12 16 Congo 580 703 727 829 418 475 474 142 201 91 111 894 1005 717 873 398 300 189 182 87 87 61 39 20 21 36 18 15 24 17 Côte d'Ivoire 365 349 456 260 206 326 240 185 121 104 188 92 97 68 74 42 29 13 14 8 8 10 9 7 6 3 0 3 2 1 Democratic Republic of the Congo 7515 5825 7757 11384 19021 18182 19342 25094 26318 18684 16951 17300 13816 11459 10339 10249 8013 8155 7318 7178 5624 5590 5968 5647 3205 2351 1769 1110 660 604 Equatorial Guinea 63 36 45 30 85 37 46 67 62 28 16 17 32 23 22 17 13 15 11 7 8 1 2 3 0 0 3 4 4 3 Gabon 80 45 33 80 61 20 32 11 6 38 45 30 26 26 49 53 31 30 24 14 22 17 9 17 10 9 10 9 16 8 Ghana 3 6 16 0 0 0 1 0 0 0 1 0 0 0 0 0 0 0 0 0 0 0 0 1 0 0 0 0 0 0 Guinea 52 29 24 27 26 33 38 88 99 68 52 72 132 130 95 94 48 69 90 79 68 57 70 78 33 29 107 140 74 69 Mali 0 0 0 27 17 11 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 Nigeria 24 0 0 0 0 0 0 0 0 27 14 14 26 31 10 21 3 0 0 0 2 3 2 0 0 0 1 0 0 0 South Sudan 67 58 28 62 69 56 157 737 1726 1312 1801 1919 3121 3061 1742 1853 789 469 623 373 199 272 317 117 63 45 17 12 17 11 Togo 2 0 0 0 0 3 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 Uganda 2066 1328 2042 1764 1469 1062 981 1123 971 1036 948 310 604 517 378 311 290 120 198 99 101 44 20 9 9 4 4 0 1 2 Total 12756 10987 14088 16607 23266 23671 28736 36585 37385 27862 25841 26095 23799 19941 17100 15624 11372 10466 10380 9680 6973 6632 7091 6228 3679 2733 2131 1420 953 864 Trypanosoma brucei rhodesiense [40] 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 2017 2018 2019 Kenya 91 8 4 2 1 0 2 5 14 22 15 10 11 0 0 0 1 0 0 1 0 0 2 0 0 0 0 0 0 0 Malawi 228 195 143 53 31 15 8 7 10 11 35 38 43 70 48 41 58 50 49 39 29 23 18 35 32 30 37 7 15 91 Mozambique 3 7 24 10 16 No data No data No data No data No data No data No data 1 No data 1 No data No data No data No data No data No data No data No data No data No data No data No data No data No data No data Uganda 1417 832 606 503 342 497 178 217 283 283 300 426 329 338 335 473 261 119 138 129 112 84 71 43 70 28 10 13 4 5 United Republic of Tanzania 187 177 366 262 319 422 400 354 299 288 350 277 228 113 159 186 127 126 59 14 5 1 4 1 1 2 3 3 0 3 Zambia 7 No data 4 1 1 1 3 No data No data 15 9 4 5 15 9 7 6 10 13 4 8 3 6 6 12 8 2 3 5 15 Zimbabwe No data No data No data No data 1 No data No data 9 No data No data No data No data No data No data No data 3 No data No data 0 3 2 4 9 1 3 3 1 1 0 2 Total 1933 1219 1147 831 710 935 591 583 606 619 709 755 617 536 552 707 453 305 259 187 154 111 101 85 115 68 52 27 24 116 History [ edit ] In 1903, David Bruce recognized the tsetse fly as the arthropod vector. ... "Rapid distribution of tryptophol (3-indole ethanol) to the brain and other tissues" . ... "The history of African trypanosomiasis" . Parasites & Vectors . 1 (1): 3. doi : 10.1186/1756-3305-1-3 . PMC 2270819 . ... "The development of drugs for treatment of sleeping sickness: a historical review" . Parasites & Vectors . 3 (1): 15. doi : 10.1186/1756-3305-3-15 . ... "The development of drugs for treatment of sleeping sickness: a historical review" . Parasites & Vectors . 3 (1): 15. doi : 10.1186/1756-3305-3-15 .

Affluenza: How to Be Successful and Stay Sane . Vermilion . ISBN 978-0-09-190011-3 . ^ James, Oliver (2008). The Selfish Capitalist . Vermilion . ISBN 978-0-09-192381-5 . ^ James, Oliver (2007). ... London: Vermilion. p. 344 . ISBN 978-0-09-190010-6 . 1. The mean prevalence of emotional distress for the six English-speaking nations combined was 21.6%. ... (Archive is the same work, but on a different website) Further reading [ edit ] The Circle of Simplicity , Cecile Andrews, ISBN 0-06-092872-7 The Golden Ghetto: The Psychology of Affluence , Jessie H. O'Neill, ISBN 978-0-9678554-0-0 Voluntary Simplicity , Duane Elgin, ISBN 0-688-12119-5 Voluntary Simplicity , Daniel Doherty & Amitai Etzioni, ISBN 0-7425-2066-8 How Much Is Too Much?

Neonatal Skin: Structure and Function . CRC Press. pp. 67–. ISBN 978-0-8247-0887-0 . ^ Mariagrazia Stracquadanio; Lilliana Ciotta (20 April 2015). ... A Woman Doctor's Guide to Skin Care: Essential Facts and Information on Keeping Skin Healthy . Hyperion. ISBN 978-0-7868-8100-0 . ^ Sarah Bekaert (2007). ... Lippincott Williams & Wilkins. pp. 328–. ISBN 978-0-7817-4059-3 . ^ Newsletter . The Academy. 1986. ^ Adrian Raine (2006). ... CUP Archive. pp. 321–. ISBN 978-0-521-22673-8 . ^ Raphael Rubin; David S. ... Academic Press. 3 October 1994. pp. 1994–. ISBN 978-0-08-058373-0 .

Glycogen storage disease type 0 Glycogen storage disease type 0 has defect in glycogen synthase Specialty Medical genetics Glycogen storage disease type 0 is a disease characterized by a deficiency in the glycogen synthase enzyme (GSY). ... Contents 1 Signs and symptoms 2 Causes 3 Pathophysiology 4 Diagnostic 4.1 Laboratory Studies 4.2 Imaging Studies 4.3 Other Tests 4.4 Procedures 4.5 Histologic Findings 4.6 Differential Diagnoses 4.7 Types 5 Treatment 6 Epidemiology 6.1 Mortality/Morbidity 6.2 Sex 6.3 Age 7 References 8 External links Signs and symptoms [ edit ] The most common clinical history in patients with glycogen-storage disease type 0 (GSD-0) is that of an infant or child with symptomatic hypoglycemia or seizures that occur before breakfast or after an inadvertent fast. ... Serum electrolytes calculate the anion gap to determine presence of metabolic acidosis ; typically, patients with glycogen-storage disease type 0 (GSD-0) have an anion gap in the reference range and no acidosis. ... Types [ edit ] There are two types of this\\e condition glycogen storage disease type 0 to be considered, they are: [3] [4] Glycogen storage disease due to liver glycogen synthase deficiency Glycogenosis due to muscle and heart glycogen synthase deficiency Treatment [ edit ] The goal for treatment of Glycogen-storage disease type 0 is to avoid hypoglycemia. ... "Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0" . J. Clin. Invest . 102 (3): 507–15. doi : 10.1172/JCI2890 .

The Hormone Decision . Contemporary Books. ISBN 978-0-07-141615-3 . ^ Maria Siemionow; Marita Eisenmann-Klein (13 January 2010). ... Rowman & Littlefield Publishers. pp. 73–. ISBN 978-0-7591-2332-8 . ^ Vasan; R.S. (1 January 1998). ... Biochemistry and Function of Sterols . CRC Press. pp. 26–27. ISBN 978-0-8493-7674-0 . ^ Michael Crocetti; Michael A. ... Lippincott Williams & Wilkins. pp. 564–. ISBN 978-0-7817-3770-8 . ^ W. Steven Pray (2006). ... Elsevier Health Sciences. pp. 1281–. ISBN 978-0-323-08678-3 . ^ Guy I. Benrubi (28 March 2012).

Lippincott Williams & Wilkins. p. 2695. ISBN 0-7817-5777-0 . ^ Miller, Neil R.; Frank Burton Walsh; Valérie Biousse; William Fletcher Hoyt (2005). ... Neurological disease and therapy. 85 . Informa Health Care. p. 204. ISBN 0-8493-3695-3 . ^ Greenberg, Mark S. (2006). ... McGraw-Hill Professional. p. 127. ISBN 0-07-105467-7 . ^ G. D. Schott (2007). ... Diagnosis and management in vision care . Butterworths. p. 16. ISBN 0-409-95082-3 . ^ a b Lee, David A.; Eve J. ... Springer. pp. 107–108. ISBN 1-84628-643-3 .

Nevus lipomatosus (cutaneous) superficialis ( NLS or NLCS , also known as "Nevus lipomatosis of Hoffman and Zurhelle" [1] ) is characterized by soft, yellowish papules or cerebriform plaques , usually of the buttock or thigh, less often of the ear or scalp, with a wrinkled rather than warty surface. [1] [2] : 625 It is usually congenital in origin or appears within the first three decades. [3] A pedunculated lipofibroma is a solitary variant of nevus lipomatosus superficialis . [3] It usually appears in adult life, and usually on the axilla, knee, ear, arm, scalp and the lower trunk. [3] Pedunculated lipofibroma, gross pathology Micrograph of pedunculated lipofibroma, low magnification, with dermal expansion of fatty tissue. ... The main differential diagnoses are acrochordon , seborrheic keratosis , intradermal melanocytic nevi , neurofibromas , verrucae and fibroepithelioma of Pinkus. [3] See also [ edit ] Skin lesion List of cutaneous conditions References [ edit ] ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . ^ a b c d Das, Anupam; Chandra, Somodyuti; Mohanty, Swosti; Gharami, RameshC; Podder, Indrashis (2015). ... Indian Journal of Paediatric Dermatology . 0 (0): 0. doi : 10.4103/2319-7250.165641 .

Lichen spinulosus Other names Keratosis spinulosa [1] : 776 Specialty Dermatology Lichen spinulosus is a rare skin disorder characterized by follicular keratotic papules that are grouped into large patches. [2] It is a variant of keratosis pilaris named for its resemblance to a patch of lichen . Contents 1 See also 2 Notes 3 References 4 External links See also [ edit ] Hook nail List of cutaneous conditions Notes [ edit ] ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... St. Louis: Mosby. ISBN 1-4160-2999-0 . References [ edit ] Friedman S (1990). ... PMID 2179296 . External links [ edit ] Derm Net NZ Emedicine Thehinhso v t e Diseases of the skin and appendages by morphology Growths Epidermal Wart Callus Seborrheic keratosis Acrochordon Molluscum contagiosum Actinic keratosis Squamous-cell carcinoma Basal-cell carcinoma Merkel-cell carcinoma Nevus sebaceous Trichoepithelioma Pigmented Freckles Lentigo Melasma Nevus Melanoma Dermal and subcutaneous Epidermal inclusion cyst Hemangioma Dermatofibroma (benign fibrous histiocytoma) Keloid Lipoma Neurofibroma Xanthoma Kaposi's sarcoma Infantile digital fibromatosis Granular cell tumor Leiomyoma Lymphangioma circumscriptum Myxoid cyst Rashes With epidermal involvement Eczematous Contact dermatitis Atopic dermatitis Seborrheic dermatitis Stasis dermatitis Lichen simplex chronicus Darier's disease Glucagonoma syndrome Langerhans cell histiocytosis Lichen sclerosus Pemphigus foliaceus Wiskott–Aldrich syndrome Zinc deficiency Scaling Psoriasis Tinea ( Corporis Cruris Pedis Manuum Faciei ) Pityriasis rosea Secondary syphilis Mycosis fungoides Systemic lupus erythematosus Pityriasis rubra pilaris Parapsoriasis Ichthyosis Blistering Herpes simplex Herpes zoster Varicella Bullous impetigo Acute contact dermatitis Pemphigus vulgaris Bullous pemphigoid Dermatitis herpetiformis Porphyria cutanea tarda Epidermolysis bullosa simplex Papular Scabies Insect bite reactions Lichen planus Miliaria Keratosis pilaris Lichen spinulosus Transient acantholytic dermatosis Lichen nitidus Pityriasis lichenoides et varioliformis acuta Pustular Acne vulgaris Acne rosacea Folliculitis Impetigo Candidiasis Gonococcemia Dermatophyte Coccidioidomycosis Subcorneal pustular dermatosis Hypopigmented Tinea versicolor Vitiligo Pityriasis alba Postinflammatory hyperpigmentation Tuberous sclerosis Idiopathic guttate hypomelanosis Leprosy Hypopigmented mycosis fungoides Without epidermal involvement Red Blanchable Erythema Generalized Drug eruptions Viral exanthems Toxic erythema Systemic lupus erythematosus Localized Cellulitis Abscess Boil Erythema nodosum Carcinoid syndrome Fixed drug eruption Specialized Urticaria Erythema ( Multiforme Migrans Gyratum repens Annulare centrifugum Ab igne ) Nonblanchable Purpura Macular Thrombocytopenic purpura Actinic/solar purpura Papular Disseminated intravascular coagulation Vasculitis Indurated Scleroderma / morphea Granuloma annulare Lichen sclerosis et atrophicus Necrobiosis lipoidica Miscellaneous disorders Ulcers Hair Telogen effluvium Androgenic alopecia Alopecia areata Systemic lupus erythematosus Tinea capitis Loose anagen syndrome Lichen planopilaris Folliculitis decalvans Acne keloidalis nuchae Nail Onychomycosis Psoriasis Paronychia Ingrown nail Mucous membrane Aphthous stomatitis Oral candidiasis Lichen planus Leukoplakia Pemphigus vulgaris Mucous membrane pemphigoid Cicatricial pemphigoid Herpesvirus Coxsackievirus Syphilis Systemic histoplasmosis Squamous-cell carcinoma This condition of the skin appendages article is a stub .

The disease usually occurs from birth to age 15. [3] Histiocytosis (and malignant histiocytosis ) are both important in veterinary as well as human pathology. Contents 1 Types 2 Diagnosis 2.1 Classification 3 Treatments 4 Society 5 References 6 External links Types [ edit ] Types of LCH have also been known as "eosinophilic granuloma", "Hand-Schuller-Christian disease", "Letterer-Siwe disease", and "histiocytosis X". ... Information concerning histiocytosis and clinicians located in European countries may be found in many languages at the web portal of Euro Histio Net (EHN). This is a project funded by the European Union, coordinated by Jean Donadieu, APHP , Paris, France. ... Andrews' Diseases of the Skin: clinical Dermatology . Saunders Elsevier. ISBN 0-7216-2921-0 . ^ Goldberg, J; Nezelof, C (1986), "Lymphohistiocytosis: a multi-factorial syndrome of macrophagic activation clinico-pathological study of 38 cases", Hematol Oncol , 4 (4): 275–289, PMID 3557322 . ^ Egan, Caoimhe; Jaffe, Elaine S. (2018). ... Springer Science & Business Media. p. 383. ISBN 978-0-387-73743-0 . External links [ edit ] Classification D ICD - 10 : C96.1 , D76.0 ICD - 9-CM : 202.3 , 277.89 MeSH : D015614 SNOMED CT : 60657004 External resources MedlinePlus : 000068 eMedicine : ped/1997 v t e Histiocytosis WHO-I/ Langerhans cell histiocytosis / X-type histiocytosis Letterer–Siwe disease Hand–Schüller–Christian disease Eosinophilic granuloma Congenital self-healing reticulohistiocytosis WHO-II/ non-Langerhans cell histiocytosis / Non-X histiocytosis Juvenile xanthogranuloma Hemophagocytic lymphohistiocytosis Erdheim-Chester disease Niemann–Pick disease Sea-blue histiocyte Benign cephalic histiocytosis Generalized eruptive histiocytoma Xanthoma disseminatum Progressive nodular histiocytosis Papular xanthoma Hereditary progressive mucinous histiocytosis Reticulohistiocytosis ( Multicentric reticulohistiocytosis , Reticulohistiocytoma ) Indeterminate cell histiocytosis WHO-III/ malignant histiocytosis Histiocytic sarcoma Langerhans cell sarcoma Interdigitating dendritic cell sarcoma Follicular dendritic cell sarcoma Ungrouped Rosai–Dorfman disease

Nevus comedonicus (also known as a " comedo nevus " [1] ) is characterized by closely arranged, grouped, often linear, slightly elevated papules that have at their center keratinous plugs resembling comedones . [2] : 634 [3] : 774 See also [ edit ] Nevus comedonicus syndrome Skin lesion List of cutaneous conditions References [ edit ] ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... Louis: Mosby. p. 1673. ISBN 1-4160-2999-0 . ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 . This Epidermal nevi, neoplasms, cysts article is a stub .

Pterygium inversum unguis Other names Pterygium inversus unguis, [1] and Ventral pterygium [2] : 660 Specialty Dermatology Pterygium inversum unguis is characterized by the adherence of the distal portion of the nailbed to the ventral surface of the nail plate. [3] : 788 The condition may be present at birth or acquired, and may cause pain with manipulation of small objects, typing, and close manicuring of the nail. [3] : 788 secondary due to connective tissue disorders See also [ edit ] Pterygium unguis Nail Anatomy List of cutaneous conditions References [ edit ] ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 . ^ a b James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . This condition of the skin appendages article is a stub .

Sex Crimes and Paraphilia . Prentice Hall . p. 91. ISBN 0-13-170350-1 . ^ Thompson, Steven L. ... Westport, Connecticut: Praeger . p. 446. ISBN 978-0-313-30503-0 . ^ Kolocotroni, Vassiliki; Goldman, Jane ; Taxidou, Olga (1998). ... Waterloo, Ontario: Wilfrid Laurier University Press . ISBN 978-0-88920-512-3 . ^ Miller, Alan (1999). ... New York City: Springer . ISBN 978-0-387-98499-5 . ^ McDonagh, Deana; et al. (2004). ... London: Taylor & Francis . ISBN 978-0-415-30363-7 . ^ Heller, Steven ; Meggs, Philip B. (2001).

As a result of quarantine procedures, some of the post-SARS patients have been documented as suffering from post-traumatic stress disorder (PTSD) and major depressive disorder . [31] [32] Epidemiology [ edit ] Main article: 2002–2004 SARS outbreak SARS was a relatively rare disease; at the end of the epidemic in June 2003, the incidence was 8,422 cases with a case fatality rate (CFR) of 11%. [4] The case fatality rate (CFR) ranges from 0% to 50% depending on the age group of the patient. [9] Patients under 24 were least likely to die (less than 1%); those 65 and older were most likely to die (over 55%). [33] As with MERS and COVID-19 , SARS resulted in significantly more deaths of males than females. 2003 Probable cases of SARS – worldwide Probable cases of SARS by country or region, 1 November 2002 – 31 July 2003 [34] Country or region Cases Deaths Fatality (%) China [a] 5,327 349 6.6 Hong Kong 1,755 299 17.0 Taiwan [b] 346 73 [35] [36] 21.1 Canada 251 43 17.1 Singapore 238 33 13.9 Vietnam 63 5 7.9 United States 27 0 0 Philippines 14 2 14.3 Thailand 9 2 22.2 Germany 9 0 0 Mongolia 9 0 0 France 7 1 14.3 Australia 6 0 0 Malaysia 5 2 40.0 Sweden 5 0 0 United Kingdom 4 0 0 Italy 4 0 0 Brazil 3 0 0 India 3 0 0 South Korea 3 0 0 Indonesia 2 0 0 South Africa 1 1 100.0 Colombia 1 0 0 Kuwait 1 0 0 Ireland 1 0 0 Macao 1 0 0 New Zealand 1 0 0 Romania 1 0 0 Russia 1 0 0 Spain 1 0 0 Switzerland 1 0 0 Total excluding China [a] 2,769 454 16.4 Total (29 territories) 8,096 774 9.6 ^ a b Figures for China exclude Hong Kong and Macau, which are reported separately by the WHO . ^ After 11 July 2003, 325 Taiwanese cases were 'discarded'. ... NHS Choices . UK National Health Service . 3 October 2014. Archived from the original on 11 March 2016 . ... Archived from the original on 26 January 2013 . Retrieved 3 August 2013 . ^ Monaghan KJ (2004). ... Archived from the original on 14 June 2007 . Retrieved 3 May 2013 . ^ "SARS death leads to China dispute" . ... Archived from the original on 28 November 2007 . Retrieved 3 April 2007 . ^ Fong K (16 August 2013).

A related term is tangentiality —it refers to off-the-point, oblique or irrelevant answers given to questions. [1] In some studies on creativity , knight's move thinking , while it describes a similarly loose association of ideas, is not considered a mental disorder or the hallmark of one; it is sometimes used as a synonym for lateral thinking . [3] [4] [5] Examples [ edit ] "The next day when I'd be going out you know, I took control, like uh, I put bleach on my hair in California." ... Bleuler in 1950. [8] The phrase knight's move thinking was first used in the context of pathological thinking by the psychologist Peter McKellar in 1957, who hypothesized that individuals with schizophrenia fail to suppress divergent associations. [3] Derailment was used with this meaning by Kurt Schneider in 1959. [8] See also [ edit ] Nonsense Non sequitur (logic) and Non sequitur (literary device) Red herring Relevance logic Schizophasia SCIgen , a program that generates nonsense research papers by grammatically combining snippets; many of the sentences generated are individually plausible Tip-of-the-tongue Train of thought References [ edit ] ^ a b P.J. McKenna, Schizophrenia and related syndromes , Psychology Press, 1997, ISBN 0-86377-790-2 , pp. 14-15 ^ a b A.C.P. Sims, Symptoms in the mind: an introduction to descriptive psychopathology , Edition 3, Elsevier Health Sciences, 2003, ISBN 0-7020-2627-1 , pp. 155-156 ^ a b Robert Spillane, John Martin, Personality and performance: foundations for managerial psychology , UNSW Press, 2005 ISBN 0-86840-816-6 , pp. 239-243 ^ Tudor Rickards, Creativity and problem solving at work , Edition 3, Gower Publishing, 1997, ISBN 0-566-07961-5 , p. 81 ^ Richard Courtney, Drama and intelligence: a cognitive theory , McGill-Queen's Press, 1990, ISBN 0-7735-0766-3 , p. 128 ^ Andreasen NC. ... CS1 maint: archived copy as title ( link ) ^ a b Tony Thompson, Peter Mathias, Jack Lyttle, Lyttle's mental health and disorder , Edition 3, Elsevier Health Sciences, 2000, ISBN 0-7020-2449-X , pp. 136, 168-170

This subgroup of the TSEs in captive animals was identified in zoo animals in Great Britain including species of greater kudu , nyala , gemsbok , the common eland , Arabian and Scimitar Oryx , an Ankole-Watusi cow, and an American bison . [1] Studies indicate that transmission likely occurred via the consumption of feed supplemented with meat and bone meal , although some animals died after the British ban on ground offal in animal feed. [2] [3] All animals died during the 1990s, with the last death occurring in 1998. [3] References [ edit ] ^ Contreras, Marcela; Barbara, John A. ... Cambridge, UK: Cambridge University Press. p. 141. ISBN 0-521-45393-3 . ^ Strauss, Ellen G.; Strauss, James H. (2008). ... Boston, MA: Elsevier / Academic Press. ISBN 0-12-373741-9 . ^ a b Baird-Parker, A. ... Gaithersburg, Md: Aspen Publishers. pp. 1590–1598. ISBN 0-8342-1323-0 . v t e Prion diseases and transmissible spongiform encephalopathy Prion diseases in humans inherited/ PRNP : fCJD Gerstmann–Sträussler–Scheinker syndrome Fatal familial insomnia sporadic: sCJD Sporadic fatal insomnia Variably protease-sensitive prionopathy acquired/ transmissible: iCJD vCJD Kuru Prion diseases in other animals Bovine spongiform encephalopathy Camel spongiform encephalopathy Scrapie Chronic wasting disease Transmissible mink encephalopathy Feline spongiform encephalopathy Exotic ungulate encephalopathy This veterinary medicine –related article is a stub .

Cambridge University Press. pp. 214 ff . ISBN 0-521-39514-3 . ^ a b Alan Felthous, Henning Sass (2008). ... John Wiley & Sons. p. 11. ISBN 978-0-470-06638-6 . ^ Ann-Louise Shapiro (1996). ... Stanford University Press. p. 100. ISBN 0-8047-2693-0 . ^ Daniel Hack Tuke (1892). ... University of Chicago Press. p. 155. ISBN 0-226-30161-3 . ^ a b Lennard J. Davis (2008). ... McGraw-Hill Professional. p. 226. ISBN 0-8442-8393-2 . ^ Susan Bordo (1996).

Bullous drug reaction Other names Bullous drug eruption, [1] generalized bullous fixed drug eruption, multilocular bullous fixed drug eruption [2] : 554 Specialty Dermatology Bullous drug reaction most commonly refers to a drug reaction in the erythema multiforme group. [3] : 129 These are uncommon reactions to medications, with an incidence of 0.4 to 1.2 per million person-years for toxic epidermal necrolysis and 1.2 to 6.0 per million person-years for Stevens–Johnson syndrome . [3] : 129 The primary skin lesions are large erythemas (faintly discernible even after confluence), most often irregularly distributed and of a characteristic purplish-livid color, at times with flaccid blisters. [2] : 554 See also [ edit ] Skin lesion List of cutaneous conditions References [ edit ] ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 . ^ a b James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . External links [ edit ] Classification D External resources eMedicine : article/1062790 This cutaneous condition article is a stub .

Acrokeratoelastoidosis of Costa Other names Keratoelastoidosis marginalis [1] Autosomal dominant is the inheritance manner for this condition Specialty Dermatology Acrokeratoelastoidosis of Costa is a familial condition characterized by multiple keratotic papules on the dorsum of the hands and feet, palms, soles, in which electron microscopy shows rarified, abnormal elastic tissue. [2] : 993 [3] : 214 It was characterized in 1953. [4] Treatments such as liquid nitrogen , salicylic acid , tretinoin , and prednisone have been tried, though with limited success. [5] See also [ edit ] Skin lesion List of cutaneous conditions References [ edit ] ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 . ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . ^ Costa OG (1953). "Akrokerato-elastoidosis; a hitherto undescribed skin disease". Dermatologica . 107 (3): 164–8. doi : 10.1159/000256794 .

Keratosis follicularis spinulosa decalvans Other names Siemens-1 syndrome Keratosis follicularis spinulosa decalvans is a rare X-linked disorder described by Siemens in 1926, a disease that begins in infancy with keratosis pilaris localized on the face, then evolves to more diffuse involvement. [1] : 580,762 [2] : 649,714 [3] An association with SAT1 has been suggested. [4] See also [ edit ] Keratosis follicularis Hermann Werner Siemens Cicatricial alopecia List of cutaneous conditions References [ edit ] ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 . ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... "Gene dosage of the spermidine/spermine N(1)-acetyltransferase ( SSAT) gene with putrescine accumulation in a patient with a Xp21.1p22.12 duplication and keratosis follicularis spinulosa decalvans (KFSD)". Hum Genet . 111 (3): 235–41. doi : 10.1007/s00439-002-0791-6 .

Pili annulati Specialty Medical genetics Pili annulati (also known as " ringed hair " [1] ) is a genetic trait in which the hair seems ‘banded‘ by alternating segments of light and dark color when seen in reflected light. [1] [2] : 767 [3] : 640 [4] See also [ edit ] Pili pseudoannulati List of cutaneous conditions References [ edit ] ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). ... St. Louis: Mosby. ISBN 1-4160-2999-0 . ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology . (10th ed.). Saunders. ISBN 0-7216-2921-0 . ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 . ^ http://www.omim.org/entry/180600 External links [ edit ] Hair Transplant Classification D ICD - 10 : Q84.1 ( ILDS Q84.110) ICD - 9-CM : 757.4 MeSH : C537187 v t e Congenital malformations and deformations of skin appendages Nail disease Anonychia Leukonychia Pachyonychia congenita / Onychauxis Koilonychia Hair disease hypotrichosis /abnormalities: keratin disease Monilethrix IBIDS syndrome Sabinas brittle hair syndrome Pili annulati Pili torti Uncombable hair syndrome Björnstad syndrome Giant axonal neuropathy with curly hair hypertrichosis : Zimmermann–Laband syndrome This condition of the skin appendages article is a stub .