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PROP1 gene mutations in a 36-year-old female presenting with psychosis

SUMMARY: Combined pituitary hormonal deficiency (CPHD) is a rare disease that results from mutations in genes coding for transcription factors that regulate the differentiation of pituitary cells. PROP1 gene mutations are one of the etiological diagnoses of congenital panhypopituitarism, however sym...

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Detalles Bibliográficos
Publicado en:Endocrinol Diabetes Metab Case Rep
Autores principales: Chaudhary, Durgesh Prasad, Rijal, Tshristi, Jha, Kunal Kishor, Saluja, Harpreet
Formato: Artigo
Lenguaje:Inglês
Publicado: Bioscientifica Ltd 2017
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5404466/
https://ncbi.nlm.nih.gov/pubmed/28458894
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-16-0096
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