Phylloid pattern of pigmentary disturbance in a case of complex mosaicism

American Journal of Medical Genetics

Volumn 98, Issue 2, 2001, Pages 145-147

  Noce, Thelma Ribeiro ^a   De Pina Neto, João Monteiro ^a   Happle, Rudolf ^b  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Hyperpigmentation; Hypopigmentation; Mosaicism; Multisystem birth defect; Phylloid pattern; Pigmentary disorder

Indexed keywords

ARTICLE; BIRTH DEFECT; CASE REPORT; CELL LINE; CHILD; CHROMOSOME MOSAICISM; CLEFT LIP; COLOBOMA; FEMALE; HUMAN; HYPERPIGMENTATION; HYPOMELANOSIS; KARYOTYPE 46,XX; MENTAL DEFICIENCY; MICROCEPHALY; MULTIPLE MALFORMATION SYNDROME; PIGEON THORAX; PIGMENT DISORDER; PRIORITY JOURNAL; SKIN FIBROBLAST;

ABNORMALITIES, MULTIPLE; ADULT; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 13; CYTOGENETICS; FEMALE; HUMANS; HYPOPIGMENTATION; MELANINS; MELANOSIS; MOSAICISM; SKIN; X CHROMOSOME;

EID: 0035863597     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010115)98:2<145::AID-AJMG1023>3.0.CO;2-7     Document Type: Article

References (5)

1. Sur un syndrome pigmentaire congénital, proche de l'incontinentia pigmenti (Bloch-Sulzberger) avec oligophrénie et malformations ostéo-articulaires multiples
2. Pigmentary patterns associated with human mosaicism: A proposed classification
3. Phylloid pigmentary pattern with mosaic trisomy 13
4. Pigmentary dysplasias and chromosomal mosaicism: Report of 9 cases
5. Pigmentary abnormalities in trisomy of chromosome 13