Carregant...
SUN-518 Sanjad Sakati Syndrome - A Rare Cause Of Congenital Hypoparathyroidism And Severe Short Stature - A Case Report
BACKGROUND: Sanjad-Sakati Syndrome (SSS) is a rare autosomal recessive disorder characterized by congenital hypoparathyroidism, dysmorphic facial features, short stature, and developmental delays (1). SSS has been reported primarily in individuals of Middle Eastern ancestry. Children are born with f...
Guardat en:
| Publicat a: | J Endocr Soc |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Endocrine Society
2019
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6552800/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-SUN-518 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|