Korean J Dermatol.  2006 May;44(5):624-626.

Incontinentia Pigmenti in a Male Infant

Affiliations
  • 1Department of Dermatology, Dongguk University International Hospital, Goyang, Korea.
  • 2Department of Dermatology, Seoul National University College of Medicine, Korea. oskwon@snu.ac.kr
  • 3Department of Dermatology, Boramae Hospital, Seoul, Korea.

Abstract

Incontinentia pigmenti (IP) is an uncommon genodermatosis that occurs mostly in female infants, but is rarely found in male infants. Male patients with incontinentia pigmenti are usually more severely affected than their female counterparts. IP is characterized by ectodermal, mesodermal, neurological, ocular, and dental manifestations. Herein, we report a case of IP in a male infant who presented with a typical course of skin manifestation, dental defects, and recurrent partial seizures. However, he did not show any signs or symptoms for ocular or cardiovascular anomalies.

Keyword

Bloch-Sulzberger syndrome; Incontinentia pigmenti

MeSH Terms

Ectoderm
Female
Humans
Incontinentia Pigmenti*
Infant*
Male*
Mesoderm
Seizures
Skin Manifestations
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