Sakati syndrome

Sanjad-Sakati syndrome is a rare autosomal recessive genetic condition seen in offspring of Middle Eastern origin. It was first described in Saudi Arabia, but has been seen in Qatari, Kuwaiti, Omani and other children from the Middle East as well as elsewhere. [Source: Wikipedia ]

Synonyms
Acrocephalopolysyndactyly type 3
Sakati-Nyhan syndrome
Sakati-Nyhan-Tisdale syndrome
OrphaNet reference
Sakati-Nyhan syndrome 
May Cause
Alopecia
Brachydactyly
Craniosynostosis
Cryptorchidism
External ear malformation
Micropenis
Skin aplasia
Skin atrophy
Skin hypoplasia
Syndactyly