Sakati-Nyhan syndrome

Sakati-Nyhan syndrome

 [sah-kah´te ni´han]
a hereditary autosomal dominant disorder characterized by conical deformity of the head, extra fingers or toes, webbed fingers and toes, hypoplastic tibias, and deformed, displaced fibulas. Called also acrocephalopolysyndactyly, type III.
Miller-Keane Encyclopedia and Dictionary of Medicine, Nursing, and Allied Health, Seventh Edition. © 2003 by Saunders, an imprint of Elsevier, Inc. All rights reserved.


William Leo, U.S. pediatrician, 1926–.
Lesch-Nyhan syndrome - see under Lesch
Sakati-Nyhan syndrome - see under Sakati
Sakati-Nyhan-Tisdale syndrome - Synonym(s): Sakati-Nyhan syndrome


Nadia, 20th century Saudi Arabian pediatrician.
Sakati syndrome - Synonym(s): Sakati-Nyhan syndrome
Sakati-Nyhan syndrome - rare syndrome, usually sporadic, featuring craniofacial defects, abnormal limbs, congenital heart defects, patchy alopecia with atrophic skin above the ears, and linear scarlike lesions in the submental areas. Synonym(s): Sakati-Nyhan-Tisdale syndrome; Sakati-syndrome
Sakati-Nyhan-Tisdale syndrome - Synonym(s): Sakati-Nyhan syndrome
Sanjad-Sakati syndrome - see under Sanjad
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