Dandy-Walker malformation in methylmalonic acidemia: a rare case report

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2431

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Dandy-Walker malformation in methylmalonic acidemia: a rare case report ; volume:21 ; number:1 ; day:13 ; month:9 ; year:2021 ; pages:1-4 ; date:12.2021
BMC pediatrics ; 21, Heft 1 (13.9.2021), 1-4, 12.2021

Creator: Liu, Jingwei
Liu, Zhuohang
Yan, Haibo
Li, Yumei

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12887-021-02874-y

URN: urn:nbn:de:101:1-2021112418135995798692

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:34 AM CEST

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Liu, Jingwei
Liu, Zhuohang
Yan, Haibo
Li, Yumei
SpringerLink (Online service)

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Dandy-Walker malformation in methylmalonic acidemia: a rare case report

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Other Objects (12)

RARE ASSOCIATION OF DOWN SYNDROME WITH DANDY WALKER MALFORMATION

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Extensive intracranial calcification of pseudo-TORCH syndrome with features of Dandy–Walker malformation

The Dandy-Walker syndrome

A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation

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Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions

Cochlear implantation in patient with Dandy-walker syndrome

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Revisiting dandy–Walker malformation with associated neurofibromatosis

Dandy Walker malformation variant associated with refractory seizures in a 6-month-old baby: case report

Extensive intracranial calcification of pseudo-TORCH syndrome with features of Dandy–Walker malformation

The Dandy-Walker syndrome

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Correction: Chromosome 16p11.2 microdeletion syndrome with microcephaly and Dandy-Walker malformation spectrum: expanding the known phenotype

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Dandy Walker malformation variant associated with refractory seizures in a 6-month-old baby: case report

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A novel intragenic deletion in OPHN1 in a Japanese patient with Dandy-Walker malformation

A fetopathological and clinical study of the Dandy-Walker malformation and a literature review

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Cochlear implantation in patient with Dandy-walker syndrome

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