Olmsted syndrome.
Article
in English
| IMSEAR
| ID: sea-1216
ABSTRACT
Olmsted syndrome is a rare disorder characterized by symmetrical sharply marginated mutilating keratoderma of palms & soles & hyperkeratotic plaques around the body orifices, onychodystrophy, ainhum & amputation of digital phalanges, flextion deformities of the fingers, localized alopecia, leukokeratosis of the tongue, shortness of stature & laxity of large joints. Inheritance is autosomal dominant, although sporadic cases have been reported. Here we describe two cases of this rare disorder with thickened hyperkeratotic lesion over palm & soles & along with amputation of 3rd , 4th & 5th toes in one case. In one of our case (case no. 2) the immediate younger brother has got the same disease. Both of them were treated with tab. Neotegason 25 mg orally daily for 3 months & there was significant improvement after treatment.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Skin
/
Syndrome
/
Congenital Abnormalities
/
Female
/
Humans
/
Male
/
Adolescent
/
Keratoderma, Palmoplantar
/
Adult
/
Joint Instability
Language:
English
Year:
2007
Type:
Article
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