Challenges in diagnosis and management of neonatal hyperparathyroidism in a resource-limited country: a case series from a Sudanese family

Neonatal hyperparathyroidism is a rare disease caused by a homozygous inactivating mutation in the calcium sensing receptor gene. It presents early in life with life threatening manifestations of hypercalcemia, if left untreated the condition may be lethal. This is the first case series reported fro...

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Detalles Bibliográficos
Autores principales: Hassan, Samar Sabir, Kempers, Marlies, Lugtenberg, Dorien, Abdallah, Asmahan Tajelsir, Musa, Salwa Abdelbagi, Ibrahim, Areej Ahmed, Abdullah, Mohamed Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2021
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627147/
https://www.ncbi.nlm.nih.gov/pubmed/34887979
http://dx.doi.org/10.11604/pamj.2021.40.105.29527

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8627147/
https://www.ncbi.nlm.nih.gov/pubmed/34887979
http://dx.doi.org/10.11604/pamj.2021.40.105.29527

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