Ellis-Van Creveld Syndrome and Dandy-Walker Malformation: An Uncommon Association.

Boujtat, Khadija; Rouf, Siham; Boutahar, Imane; Skiker, Imane; Tajir, Mariam; Latrech, Hanane

Boujtat, Khadija; Rouf, Siham; Boutahar, Imane; Skiker, Imane; Tajir, Mariam; Latrech, Hanane.

Afiliação

Boujtat K; Department of Endocrinology, Mohammed VI Hospital, Medical School, Mohamed the First University, Oujda, Morocco.
Rouf S; Department of Endocrinology, Mohammed VI Hospital, Medical School, Mohamed the First University, Oujda, Morocco.
Boutahar I; Department of Radiology, Mohammed VI Hospital, Medical School, Mohamed the First University, Oujda, Morocco.
Skiker I; Department of Radiology, Mohammed VI Hospital, Medical School, Mohamed the First University, Oujda, Morocco.
Tajir M; Laboratory of Medical Genetics, Mohammed VI Hospital, Medical School, Mohamed the First University, Oujda, Morocco.
Latrech H; Medical School, Mohammed VI Hospital 4806, 60049 Oujda, Morocco, E-mail: hlatrech@hotmail.fr.

Pediatr Endocrinol Rev ; 16(2): 275-283, 2018 Dec.

Article em En | MEDLINE | ID: mdl-30556660

Assuntos

Síndrome de Dandy-Walker; Síndrome de Ellis-Van Creveld; Polidactilia; Sistema Nervoso Central; Criança; Humanos; Rim; Masculino

Palavras-chave

Chondroectodermal dysplasia; Dandy-Walker malformation; Ellis-Van Creveld syndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Ellis-Van Creveld / Polidactilia / Síndrome de Dandy-Walker Tipo de estudo: Risk_factors_studies Limite: Child / Humans / Male Idioma: En Revista: Pediatr Endocrinol Rev Assunto da revista: ENDOCRINOLOGIA / PEDIATRIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Marrocos País de publicação: Israel

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