Incontinentia pigmenti in an infant

Journal of Pediatrics

Volumn 149, Issue 1, 2006, Pages 138-

  Leung, Alexander K C ^a   Kao, C Pion ^a   Robson, Wm Lane M ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; ERYTHEMA; FEMALE; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; HYPERPIGMENTATION; INCONTINENTIA PIGMENTI; INFANT; INFANT DISEASE; PRIORITY JOURNAL; PUSTULE; SKIN MANIFESTATION; SYMPTOM; TONIC CLONIC SEIZURE; X CHROMOSOME LINKED DISORDER;

FEMALE; HUMANS; INCONTINENTIA PIGMENTI; INFANT; SEIZURES;

EID: 33745955826     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2005.12.022     Document Type: Article

References (6)

1. Ciarallo L. Two cases of incontinentia pigmenti simulating child abuse. Pediatrics 100 (1997) e6
2. Hadj-Rabia S., Froidevaux D., Bodak N., et al. Clinical study of 40 cases of incontinentia pigmenti. Arch Dermatol 139 (2003) 1163-1170
3. Happle R. A fresh look at incontinentia pigmenti. Arch Dermato 139 (2003) 1206-1207
4. Stitt W.Z., Scott G.A., Caserta M., and Goldsmith L.A. Coexistence of incontinentia pigmenti and neonatal herpes simplex virus infection. Pediatr Dermatol 2 (1998) 112-115
5. Roberts W.M., Jenkins J.J., Moorhead II E.L., et al. Incontinentia pigmenti, a chromosomal instability syndrome, is associated with childhood malignancy. Cancer 62 (1988) 2370-2372
6. Rubianes E.I., Almodóvar P.I., and Sánchez J.L. Incontinentia pigmenti. Bol Asoc Med P Rico 82 (1990) 431-433