Incontinentia Pigmenti
- 1 August 1973
- journal article
- research article
- Published by SAGE Publications in Clinical Pediatrics
- Vol. 12 (7) , 396-401
- https://doi.org/10.1177/000992287301200806
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.Keywords
This publication has 15 references indexed in Scilit:
- Incontinentia PigmentiArchives of Dermatology, 1970
- Incontinentia Pigmenti: Clinical and Genetical Studies of two Familial CasesDermatology, 1970
- Retrolental Membrane Associated with Bloch-Sulzberger Syndrome (Incontinentia Pigmenti)American Journal of Ophthalmology, 1966
- Bloch-Sulzberger Syndrome (Incontinentia Pigmenti)Archives of Neurology, 1963
- Incontinentia PigmentiAmerican Journal of Ophthalmology, 1959
- A propos de l’«Incontinentia pigmenti», délimitation de deux syndromes différents figurant sous le même termeDermatology, 1954
- BULLOUS VARIETY OF INCONTINENTIA PIGMENTI (BLOCH-SULZBERGER)Archives of Dermatology, 1952
- INCONTINENTIA PIGMENTIA.M.A. Archives of Dermatology and Syphilology, 1951
- INCONTINENTIA PIGMENTI (BLOCH-SULZBERGER)Archives of Dermatology and Syphilology, 1938
- Über eine bisher nicht beschriebene congenitale PigmentanomalieArchives of Dermatological Research, 1928