Endocrinological Manifestations of Sanjad-Sakati Syndrome

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 endocrinologica...

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Bibliographic Details
Published in:Curēus (Palo Alto, CA) CA), 2020-06, Vol.12 (6), p.e8770-e8770
Main Authors: Bashar, Masharib, Taimur, Muhammad, Amreek, FNU, Sayeed, Khalid A, Tahir, Amber
Format: Article
Language:English
Subjects:
Cell division
Defects
Endocrinology/Diabetes/Metabolism
Genetics
Growth hormones
Hypothyroidism
Insulin-like growth factors
Mutation
Pathophysiology
Patients
Pediatrics
Proteins
Thyroid gland
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Summary: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.
ISSN:2168-8184
2168-8184
DOI:10.7759/cureus.8770