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Woodhouse-Sakati Syndrome: case report and symptoms review (CROSBI ID 133551)

Prilog u časopisu | stručni rad

Medica, Igor ; Sepčić, Juraj ; Peterlin, Borut Woodhouse-Sakati Syndrome: case report and symptoms review // Genetic counseling, 18 (2007), 2; 227-231-x

Podaci o odgovornosti

Medica, Igor ; Sepčić, Juraj ; Peterlin, Borut

engleski

Woodhouse-Sakati Syndrome: case report and symptoms review

We report on a 52-year old Caucasian woman exhibiting signs of Woodhouse-Sakati syndrome and review the clinical signs and symptoms in patients reported so far. The syndrome is characterized by alopecia, mental retardation, hypogonadism, diabetes mellitus, hearing impairment, ECG changes, and by autosomal recessive inheritance. We also propose that the limited mobility of the upper extremities is one of the features of the syndrome.

Woodhouse-Sakati Syndrome

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

nije evidentirano

Podaci o izdanju

18 (2)

2007.

227-231-x

objavljeno

1015-8146

Povezanost rada

Kliničke medicinske znanosti

Indeksiranost