Paradominant inheritance of twin spotting: Phacomatosis pigmentovascularis as a further possible example

European Journal of Dermatology

Volumn 13, Issue 6, 2003, Pages 612-

  Danarti, Retno ^a   Happle, Rudolf ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; CASE REPORT; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; GENODERMATOSIS; HETEROZYGOSITY LOSS; HUMAN; LETTER; MALE; NEVUS FLAMMEUS; PHACOMATOSIS PIGMENTOVASCULARIS; PHAKOMATOSIS; SIBLING; SKIN COLOR; SKIN DISEASE;

ADOLESCENT; FEMALE; HUMANS; LOSS OF HETEROZYGOSITY; MALE; MOSAICISM; NEUROCUTANEOUS SYNDROMES; NEVUS; PIGMENTATION DISORDERS; SKIN NEOPLASMS;

EID: 0346788940     PISSN: 11671122     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (4)

1. Baba M, Seçkin D, Akçali C, Happle R. Familial cutis tricolor: A possible example of paradominant inheritance. Eur J Dermatol 2003; 13: 343-5.
2. Happle R, Barbi G, Eckert D, Kennerknecht I. "Cutis tricolor": Congenital hyper-and hypopigmented macules associated with a sporadic multisystem birth defect: An unusual example of twin spotting? J Med Genet 1997; 34: 676-8.
3. Happle R, Steijlen PM. Phacomatosis pigmentovascularis gedeutet als ein Phänomen der Zwillingsflecken. Hautarzt 1989; 40: 721-4.
4. Suzuki K, Ishizaki H, Takahashi H. Phacomatosis pigmentovascularis IIIb associated with porokeratosis, acanthosis nigricans and endocrinopathy in brother and sister (In Japanese, with an English summary). Skin Res (Hifu) 1990; 32: 65-70.