Incontinentia Pigmenti-Reference-Cited by-同舟云学术

Incontinentia Pigmenti

Published:1973-08 Issue:7 Volume:12 Page:396-401
ISSN:0009-9228
Container-title:Clinical Pediatrics
language:en
Short-container-title:Clin Pediatr (Phila)

Author:

Gurevitch Arnold W.¹,Farrell William¹,Horlick Shirley¹,Hirose Frank¹,Reisner Ronald M.¹

Affiliation:

1. Departments of Medicine (Division of Dermatology), Pediatrics and Pathology, Harbor General Hospital, 1000 W. Carson St., Torrance, Ca. 90509,, UCLA School of Medicine, Los Angeles, Ca. 90024

Abstract

An infant with IP, here presented, typifies the early course of this syn drome. Diagnosis can and should be made in the first stage by a combina tion of the clinical appearance and the characteristic histology. The physician must be aware of the frequent associated manifestations, so that he may deal as effectively as possible with them. He should inform and reassure the parents as to the future self-limited course of all of the cutaneous lesions. Genetic counseling is another important responsibility.

Publisher

SAGE Publications

Subject

Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/000992287301200806

Reference16 articles.

1. Über eine bisher nicht beschriebene congenitale Pigmentanomalie

2. Incontinentia Pigmenti: Clinical and Genetical Studies of two Familial Cases

3. INCONTINENTIA PIGMENTI

4. BULLOUS VARIETY OF INCONTINENTIA PIGMENTI (BLOCH-SULZBERGER)

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