Unusual ocular manifestation in a patient with incontinentia pigmenti
نویسندگان
چکیده
منابع مشابه
Leukoencephalopathy: unusual sonographic finding in a neonate with incontinentia pigmenti.
ncontinentia pigmenti (IP) is a rare X-linked dominant neurocutaneous syndrome chiefly involving the ectodermal tissues, such as the skin, teeth, hair, eyes, and central nervous system (CNS).1 The diagnosis is usually made when the pathognomonic skin lesions are present; these typically appear in 4 stages: erythematous vesicular rash, verrucous patches, swirling hyperpigmentation, and atrophic ...
متن کاملIncontinentia pigmenti*
Incontinentia pigmenti is a rare genodermatosis in which the skin involvement occurs in all patients. Additionally, other ectodermal tissues may be affected, such as the central nervous system, eyes, hair, nails and teeth. The disease has a X-linked dominant inheritance pattern and is usually lethal to male fetuses. The dermatological findings occur in four successive phases, following the line...
متن کاملOcular anomalies in incontinentia pigmenti: literature review and meta-analysis.
INTRODUCTION Incontinentia pigmenti (IP) is an X-linked genodermatosis in which skin changes are combined with dental, eye and central nervous system anomalies. OBJECTIVE The goal of the study was to analyze ocular findings, IP minor criteria in available literature concerning IP cases published until now. METHODS We have done meta-analysis of 1931 IP patients found in 302 references publis...
متن کاملOcular changes in the Bloch-Sulzberger syndrome (Incontinentia pigmenti)
THE Bloch-Sulzberger syndrome is a familial condition consisting chiefly of ectodermal defects, of which changes in the skin, nails, hair, teeth, central nervous system, and eyes are the most common. The final dermal phase "incontinentia pigmenti" has received the most attention. This disease can be described as a rare and peculiar abnormality of development found almost exclusively in females ...
متن کامل[Incontinentia pigmenti].
Four new cases of incontinentia pigmenti are presented, including chromosome studies of one family. An increased number of chromosome breakages was found in the blood of affected as well as unaffected members of this family.
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ژورنال
عنوان ژورنال: Revista Brasileira de Oftalmologia
سال: 2018
ISSN: 0034-7280
DOI: 10.5935/0034-7280.20180046