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Syndrome of alopecia totalis and 17b-hydroxysteroid dehydrogenase deficiency
A Kauschansky1, M Shohat, M Frydman
1Institute for Pediatric and Adolescent Endocrinology, Schneider Children's Medical Center of Israel, Beilinson Campus, Petah Tiqva.
American Journal of Medical Genetics
|March 21, 1998
Abstract:
A distinct and previously undescribed syndrome of alopecia totalis, ichthyosis, and male pseudohermaphroditism due to steroid 17b-hydroxysteroid dehydrogenase deficiency was observed in an Israeli-Arab newborn infant.