LymphedemaV1, Istex, Corpus, bibRecord, 003483

Surviving male with incontinentia pigmenti: a case report

Identifieur interne : 003483 ( Istex/Corpus ); précédent : 003482; suivant : 003484

Surviving male with incontinentia pigmenti: a case report

Auteurs : S. Y. Cho ; C. K. Lee ; B. K. Drummond

Source :

International Journal of Paediatric Dentistry [ 0960-7439 ] ; 2004-01.

RBID : ISTEX:70FCCFFC71A5397CB0B306E06B5581D5A4AEABF6

Abstract

Summary. Incontinentia pigmenti, or Block–Sulzberger Syndrome, is an X‐linked dominant disorder with characteristic skin, hair, eye and tooth abnormalities. It is classically considered a male‐lethal disorder with recurrent miscarriages of male foetuses. A few cases of surviving males with incontinentia pigmenti have been reported in the medical literature. This article reports the medical and dental findings of a boy diagnosed with incontinentia pigmenti.

Url:

https://api.istex.fr/document/70FCCFFC71A5397CB0B306E06B5581D5A4AEABF6/fulltext/pdf

DOI: 10.1111/j.1365-263X.2004.00516.x

Links to Exploration step

ISTEX:70FCCFFC71A5397CB0B306E06B5581D5A4AEABF6

Le document en format XML

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Surviving male with incontinentia pigmenti: a case report

Surviving male with incontinentia pigmenti: a case report

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