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Literature DB >> 1002140

Expansion and contraction of hypomelanotic areas in human piebaldism.

Abstract

A case of human piebaldism with white forelock is presented, with emphasis on the unusual aspect of expansion and diminution of the hypomelanotic areas. Possible mechanisms of piebaldism and of changes in the hypomelanotic areas are discussed.

Entities: Disease Species

Mesh：

Year: 1976 PMID： 1002140 DOI： 10.1007/bf00278885

Source DB: PubMed Journal: Hum Genet ISSN： 0340-6717 Impact factor: 4.132

10 in total

1. ELECTRON MICROSCOPY OF MELANOCYTES IN HUMAN PIEBALDISM.

Authors: A S BREATHNACH; T B FITZPATRICK; L M WYLLIE
Journal: J Invest Dermatol Date: 1965-07 Impact factor: 8.551

2. Further studies on the phenomenon of pigment spread in guinea pigs' skin.

Authors: R E BILLINGHAM; W K SILVERS
Journal: Ann N Y Acad Sci Date: 1963-02-15 Impact factor: 5.691

3. Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects.

Authors: A M DIGEORGE; R W OLMSTED; R D HARLEY
Journal: J Pediatr Date: 1960-11 Impact factor: 4.406

4. Piebaldness, of familial white skin spotting; partial albinism.

Authors: H M JAHR; M S McINTIRE
Journal: AMA Am J Dis Child Date: 1954-10

5. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

Authors: P J WAARDENBURG
Journal: Am J Hum Genet Date: 1951-09 Impact factor: 11.025

1 in total

1. Magdeleine of Martinique.

Authors: G E Gifford
Journal: Int J Dermatol Date: 1980-03 Impact factor: 2.736

1 in total

Expansion and contraction of hypomelanotic areas in human piebaldism.

1. ELECTRON MICROSCOPY OF MELANOCYTES IN HUMAN PIEBALDISM.

2. Further studies on the phenomenon of pigment spread in guinea pigs' skin.

3. Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects.

4. Piebaldness, of familial white skin spotting; partial albinism.

5. A new syndrome combining developmental anomalies of the eyelids, eyebrows and nose root with pigmentary defects of the iris and head hair and with congenital deafness.

6. Familial white skin spotting (piebaldness) ("partial albinism") with white forelock.

7. Dominant piebald trait (white forelock and leukoderma) with neurological impairment.

8. The development of piebald spotting in mice.

9. Partial albinism.

10. Studies on the migratory behavior of melanocytes in guinea pig skin.

1. Magdeleine of Martinique.