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Rare Coexistence of Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency and Turner Syndrome: A Case Report and Brief Literature Review
Inácio, Isabel; Serra-Caetano, Joana; Cardoso, Rita; Dinis, Isabel; Mirante, Alice.
Affiliation
  • Inácio I; Centro Hospitalar do Baixo Vouga, Department of Endocrinology, Aveiro, Portugal
  • Serra-Caetano J; Hospital Pediátrico de Coimbra, Department of Paediatric Endocrinology, Diabetes and Growth, Coimbra, Portugal
  • Cardoso R; Hospital Pediátrico de Coimbra, Department of Paediatric Endocrinology, Diabetes and Growth, Coimbra, Portugal
  • Dinis I; Hospital Pediátrico de Coimbra, Department of Paediatric Endocrinology, Diabetes and Growth, Coimbra, Portugal
  • Mirante A; Hospital Pediátrico de Coimbra, Department of Paediatric Endocrinology, Diabetes and Growth, Coimbra, Portugal
J Clin Res Pediatr Endocrinol ; 15(1): 86-89, 2023 02 27.
Article in En | MEDLINE | ID: mdl-34355878
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Res Pediatr Endocrinol Year: 2023 Type: Article Affiliation country: Portugal
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Clin Res Pediatr Endocrinol Year: 2023 Type: Article Affiliation country: Portugal