Atypical presentation of a newborn with Apert syndrome.

Spruijt, B; Rijken, B F M; Joosten, K F M; Bredero-Boelhouwer, H H; Pullens, B; Lequin, M H; Wolvius, E B; van Veelen-Vincent, M L C; Mathijssen, I M J

Spruijt, B; Rijken, B F M; Joosten, K F M; Bredero-Boelhouwer, H H; Pullens, B; Lequin, M H; Wolvius, E B; van Veelen-Vincent, M L C; Mathijssen, I M J.

Affiliation

Spruijt B; Dutch Craniofacial Center, Sophia Children's Hospital-Erasmus University Medical Center, Wytemaweg 80, Room SK-1202, PO Box 2060, 3015 CN, Rotterdam, The Netherlands, b.spruijt@erasmusmc.nl.

Childs Nerv Syst ; 31(3): 481-6, 2015 Mar.

Article in En | MEDLINE | ID: mdl-25433548

Subject(s)

Acrocephalosyndactylia; Acrocephalosyndactylia/complications; Acrocephalosyndactylia/genetics; Acrocephalosyndactylia/surgery; Adult; Endoscopy; Female; Follow-Up Studies; Humans; Infant, Newborn; Intracranial Pressure; Magnetic Resonance Imaging; Male; Middle Aged; Mutation/genetics; Receptor, Fibroblast Growth Factor, Type 2/genetics; Respiration Disorders/etiology

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Full text: 1 Database: MEDLINE Main subject: Acrocephalosyndactylia Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged / Newborn Language: En Year: 2015 Type: Article

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