Cushing's disease associated with 21q22.3 deletion syndrome.

Gilmour, Leeyan S; Hunt, Penny J; Law, Andrew; Mackenzie, Karen E; de Bock, Martin

Gilmour, Leeyan S; Hunt, Penny J; Law, Andrew; Mackenzie, Karen E; de Bock, Martin.

Afiliação

Gilmour LS; Department of Paediatric Endocrinology, Christchurch Hospital, Christchurch, New Zealand.
Hunt PJ; Department of Endocrinology, Christchurch Hospital, Christchurch, New Zealand.
Law A; Department of Paediatric Neurosurgery, Starship Children's Hospital, Auckland, New Zealand.
Mackenzie KE; Department of Paediatric Endocrinology, Christchurch Hospital, Christchurch, New Zealand.
de Bock M; Department of Paediatrics, University of Otago, Christchurch, New Zealand.

J Paediatr Child Health ; 57(6): 943-946, 2021 06.

Article em En | MEDLINE | ID: mdl-32862504

Assuntos

Síndrome de Cushing; Hipersecreção Hipofisária de ACTH; Síndrome de Cushing/diagnóstico; Síndrome de Cushing/genética; Humanos

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Cushing / Hipersecreção Hipofisária de ACTH Tipo de estudo: Diagnostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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