J Korean Pediatr Soc.  1996 Sep;39(9):1315-1319.

Two Cases of Congenital Atrichia Associated with the Gastrointestinal Anomaly in Siblings

Affiliations
  • 1Department of Pediatrics, Dae Dong Hospital, Pusan, Korea.

Abstract

Congenital atrichia is an anomaly characterized by congenital absence of hair in varying degrees as well as the ypopigmentation & poor development of the abnormal residual hair on the scalp, eyebrows, eyelashes & body. Two cases of congenital atrichia in siblings were reviewed. The first case was associated with congenital megacolon and skin biopsy of scalp (esp. parietal region) was non-specific. The second case was associated with bilateral inguinal hernia. Congenital atrichia is inherited by autosomal dominant or recessive. Acording to the limited pedigree data, our cases were X-linked recessive inheritance We report these cases with a review of related literatures.

Keyword

Congenital atriclda; Congenital megacolon; Inguinal hernia

MeSH Terms

Biopsy
Eyebrows
Eyelashes
Hair
Hernia, Inguinal
Hirschsprung Disease
Humans
Pedigree
Rabeprazole
Scalp
Siblings*
Skin
Wills
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