1.
Indian J Pathol Microbiol
;
2010 Apr-Jun; 53(2): 302-304
Artículo
en Inglés
| IMSEAR
| ID: sea-141668
RESUMEN
Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome is a rare X-linked dominant genodermatosis related to the NF kappa B essential modulator (NEMO) gene with approximately 800 cases reported worldwide. It usually occurs in females characterized by cutaneous, skeletal, neurological, ocular and dental abnormalities as well as an increased risk of childhood malignancies. Herein, we report a case of IP in a 14-year-old girl emphasizing early diagnosis and adding to the current literature on the subject.
2.
Indian J Dermatol Venereol Leprol
;
2009 May-June; 75(3): 330
Artículo
en Inglés
| IMSEAR
| ID: sea-140376
3.
Indian Pediatr
;
2008 Jul; 45(7): 609-10
Artículo
en Inglés
| IMSEAR
| ID: sea-7887