Results 101 to 110 of about 2,525 (203)

Neurocutaneous syndromes with pigmentary abnormalities and central nervous system involvement. II. Two cases with atypical incontinentia pigmenti.

open access: yes, 1990
Two cases are reported of a boy and a girl with similar neurocutaneous syndromes clinically characterized by hyperpigmented skin patches and severe CNS involvement. The diagnosis of atypical cases of Incontinentia Pigmenti is suggested.
Palmeri S.   +6 more
core   +1 more source

MACULAR NEUROVASCULAR ABNORMALITIES IN A CHILD WITH INCONTINENTIA PIGMENTI ON HANDHELD OPTICAL COHERENCE TOMOGRAPHY ANGIOGRAPHY. [PDF]

open access: yesRetin Cases Brief Rep, 2023
Patel PR   +6 more
europepmc   +1 more source

Incontinentia pigmenti – a case report

open access: yes, 2012
Introdução: A Incontinentia pigmenti (IP) é uma rara genodermatose neuroectodérmica, com uma incidência de 1:50.000 nascimentos, sendo tipicamente letal no sexo masculino, in utero.
Matos, J.   +4 more
core  

Incontinentia pigmenti (Bloch-Sulzberger syndrome): a case report.

open access: yes, 1993
A syndrome--incontinentia pigmenti--of probable genetic etiology, is discussed and a new case report presented. The syndrome presents systemic and dental manifestations, which are separate although similar to those found in other disease entities, i.e ...
Di Nicoló, R.   +3 more
core   +1 more source

Incontinentia pigmenti presenting as pseudoretinoblastoma

open access: yesIndian Journal of Ophthalmology. Case Reports, 2021
Samuel Martin   +3 more
doaj   +1 more source

A Female Child with Skin Lesions and Seizures Case report of Incontinentia Pigmenti

open access: yesSultan Qaboos University Medical Journal, 2009
Incontinentia Pigmenti (IP), (OMIM # 308300), is a rare X-linked dominant condition. It is a multisystemic disease with neuroectodermal findings involving the skin, eyes, hair, nails, teeth, and central nervous system.
Sana Al-Zuhaibi   +5 more
doaj  

Abnormal dentition in a boy with incontinentia pigmenti: case report.

open access: yesFrontiers in Dentistry, 2012
Incontinentia pigmenti (IP) is an X-linked dominant genodermatosis characterized by typical skin lesions along Blaschko's lines and associated with ocular, dental, nails, hair, skeletal, central nervous system and cardiovascular anomalies.
H Afshar   +4 more
doaj  

The Impact of the IKBKG Gene on the Appearance of the Corpus Callosum Abnormalities in Incontinentia Pigmenti. [PDF]

open access: yesDiagnostics (Basel), 2023
Minić S   +5 more
europepmc   +1 more source

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