نتایج جستجو برای: incontinentia pigment

تعداد نتایج: 27944  

Journal: :iranian journal of child neurology 0
behnaz basiri assistant professor of neonatology, hamedan university of medical sciences ,hamedan, iran mohammad mahdi taghdiri associate professor of pediatric neurology, hamedan university of medical sciences,hamedan, iran

objective incontinentia pigmenti (ip) (bloch_sulzberg syndrome) is a rare neurocutaneous syndrome characterized by multisystemic involvement that is prenatally lethal in the majority of affected males and shows great clinical variability when expressed in women. the diagnosis of ip is performed based on clinical features and the family history with the support of histological findings. we repor...

Journal: :Military Medical and Pharmaceutical Journal of Serbia 2010

Journal: :The British journal of ophthalmology 1988
C A Brown

A case is described of incontinentia pigmenti in an infant with relatively normal retinae at seven days after birth who went on to total blindness by three months. This was due to excessive neovascularisation of retinae and vitreous, leading to bilateral pseudoglioma.

Journal: :British Journal of Ophthalmology 1988

Journal: :Anais brasileiros de dermatologia 2011
Isabella Brasil Succi Fernando Colonna Rosman Elisa Fontenelle de Oliveira

Bloch-Sulzberger syndrome (incontinentia pigmenti) is a rare genodermatosis that affects predominantly females, since it is generally lethal to male fetuses in utero. It is characterized principally by skin lesions, but may also involve dental, ophthalmological and neurological abnormalities. The skin lesions are present in four different phases: vesicular, verrucous, hyperpigmented and atrophi...

Journal: :acta medica iranica 0
maryam azizzadeh department of dermatology, semnan university of medical sciences, semnan, iran. morteza rezaei department of pediatrics, semnan university of medical sciences, semnan, iran. nargess hashemi department of pediatrics, semnan university of medical sciences, semnan, iran.

incontinentia pigmenti (ip) is a rare x-linked dominant disorder with skin, eye, central nervous system (cns) and tooth abnormalities. according to the reported cases, it is estimated that there have been nearly 900-1200 affected individuals. in this article, the literature is reviewed and a case of ip with characteristic skin lesions and optic atrophy is presented.

Journal: :Nederlands tijdschrift voor geneeskunde 1962
A P Oranje W F Arts M C Loonen V D Vuzevski T van Joost E Stolz

Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a genetic disease of the skin with generalised ectodermal and mesodermal dysplasia which may often involve the eyes (35% of the patients),' hair, teeth, and central nervous system. Skin lesions are Correspondence to Dr A Spallone. usually present at birth or shortly after in the form of erythematous eruptions with linear vesiculations. The f...

Journal: :international journal of marine science and engineering 2012
m. shapoori z. ghiasvand sh. jamili

in this study, we have investigated the effects of mix of tomato (solanum lycopersicum) & carrot) daucus carota ( and red bell pepper )capsicum annuum( as a natural pigment source and astaxanthin as synthetic pigment sources on the skin colour of cichlid fish (astronotus ocellatus sp., agassiz, 1831), which are generally white with red patches in the dorsal skin. the fish were fed diets con...

Journal: :European Journal of Human Genetics 2019

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