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Endocrinological Manifestations of Sanjad-Sakati Syndrome
Masharib Bashar1, Muhammad Taimur2, Fnu Amreek3
1Internal Medicine, Dr. Ruth KM Pfau Civil Hospital, Karachi, PAK.
Abstract:
Sanjad-Sakati syndrome (SSS), also known as hypoparathyroidism-retardation-dysmorphism (HRD) syndrome, is a very rare genetic disorder with an autosomal recessive mode of inheritance, mostly seen in children of Middle Eastern origin. Hypoparathyroidism remains the most characteristic endocrinological feature of SSS; but not the only one. This review outlines and elucidates other endocrinological manifestations that may be seen with this syndrome.
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