Congenital Combined Pituitary Hormone Deficiency Attributable to a Novel PROP1 Mutation (467insT)
J Pediatr Endocrinol Metab
.
2023 Nov 2;19(4):491-498.
doi: 10.1515/jpem-2006-190406.
Print 2006 Apr 1.
Authors
O Nose
,
K Tatsumi
,
Y Nakano
,
N Amino
PMID:
38742783
DOI:
10.1515/jpem-2006-190406
No abstract available
Publication types
Case Reports
MeSH terms
Female
Homeodomain Proteins* / genetics
Humans
Hypopituitarism* / genetics
Male
Mutation*
Prognosis