A Diagnosis to Consider in an Adult Patient with Facial Features and Intellectual Disability: Williams Syndrome.

Dogan, Özlem Akgün; Simsek Kiper, Pelin Özlem; Utine, Gülen Eda; Alikasifoglu, Mehmet; Boduroglu, Koray

Dogan, Özlem Akgün; Simsek Kiper, Pelin Özlem; Utine, Gülen Eda; Alikasifoglu, Mehmet; Boduroglu, Koray.

Afiliação

Dogan ÖA; Division of Pediatric Genetics, Department of Pediatrics, Hacettepe University, Ankara, Turkey.
Simsek Kiper PÖ; Division of Pediatric Genetics, Department of Pediatrics, Hacettepe University, Ankara, Turkey.
Utine GE; Division of Pediatric Genetics, Department of Pediatrics, Hacettepe University, Ankara, Turkey.
Alikasifoglu M; Division of Pediatric Genetics, Department of Pediatrics, Hacettepe University, Ankara, Turkey.
Boduroglu K; Division of Pediatric Genetics, Department of Pediatrics, Hacettepe University, Ankara, Turkey.

Korean J Fam Med ; 38(2): 102-105, 2017 Mar.

Article em En | MEDLINE | ID: mdl-28360987

Palavras-chave

Adult; Case Reports; Complications; Management; Williams Syndrome

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Korean J Fam Med Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Turquia País de publicação:

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