نتایج جستجو برای: poikiloderma

تعداد نتایج: 174  

Journal: :Indian journal of dermatology, venereology and leprology 1998
P K Kaviarasan P V S Prasad Shradda P Viswanathan

Kindler syndrome is a rare autosomal recessive disorder associated with skin fragility. It is characterized by blistering in infancy, photosensitivity and progressive poikiloderma. The syndrome involves the skin and mucous membrane with radiological changes. The genetic defect has been identified on the short arm of chromosome 20. This report describes an 18-year-old patient with classical feat...

Journal: :Proceedings of the Royal Society of Medicine 1931

Journal: :Our Dermatology Online 2013

Journal: :The Journal of the Association of Physicians of India 2003
P K Sharma Namita Rath S K Sharma R K Gautam H K Kar

A case of poikiloderma developed polymyositis ten years after the onset of skin changes. This rare case of poikilodermatomyositis, hitherto not reported from Asian continent, is documented.

Journal: :Proceedings of the Royal Society of Medicine 1932

2010
Lidia Larizza Gaia Roversi Ludovica Volpi

Rothmund-Thomson syndrome (RTS) is a genodermatosis presenting with a characteristic facial rash (poikiloderma) associated with short stature, sparse scalp hair, sparse or absent eyelashes and/or eyebrows, juvenile cataracts, skeletal abnormalities, radial ray defects, premature aging and a predisposition to cancer. The prevalence is unknown but around 300 cases have been reported in the litera...

Journal: :British Journal of Dermatology 2019

Journal: :Journal of medical genetics 2006
L Van Maldergem H A Siitonen N Jalkh E Chouery M De Roy V Delague M Muenke E W Jabs J Cai L L Wang S E Plon C Fourneau M Kestilä Y Gillerot A Mégarbané A Verloes

Baller-Gerold syndrome (BGS) is a rare autosomal recessive condition with radial aplasia/hypoplasia and craniosynostosis (OMIM 218600). Of >20 cases reported so far, a few appear atypical and have been reassigned to other nosologic entities, including Fanconi anaemia, Roberts SC phocomelia, and Pfeiffer syndromes after demonstration of corresponding cytogenetic or molecular abnormalities. Clini...

Journal: :Gaceta medica de Mexico 2016
Gloria María Rosales-Solis César Adrián Martínez-Longoria Guillermo Antonio Guerrero-González Jorge Ocampo-Garza Jorge Ocampo-Candiani

Bloom syndrome is an extremely rare inherited disorder. We present a case of Bloom syndrome with a chromosomal study in a Mexican five-year-old patient who presented growth retardation, narrow facies with poikiloderma, café-au-lait, macules and photosensitivity.

Journal: :Proceedings of the Royal Society of Medicine 1947

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