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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Detalles Bibliográficos
Autores principales: Bashar, Masharib, Taimur, Muhammad, Amreek, FNU, Sayeed, Khalid A, Tahir, Amber
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Endocrinology/Diabetes/Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7377659/
https://www.ncbi.nlm.nih.gov/pubmed/32714707
http://dx.doi.org/10.7759/cureus.8770
Descripción
Sumario: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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