Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)- the new lacunae: a case report
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)- the new lacunae: a case report ; volume:24 ; number:1 ; day:26 ; month:8 ; year:2024 ; pages:1-6 ; date:12.2024
BMC ophthalmology ; 24, Heft 1 (26.8.2024), 1-6, 12.2024
- Urheber
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Silva, Nuno Álvaro
Silva, Renato Emílio Santos
Magalhães, António Augusto
- Beteiligte Personen und Organisationen
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SpringerLink (Online service)
- DOI
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10.1186/s12886-024-03627-y
- URN
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urn:nbn:de:101:1-2411112101150.955597553370
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:22 MESZ
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Beteiligte
- Silva, Nuno Álvaro
- Silva, Renato Emílio Santos
- Magalhães, António Augusto
- SpringerLink (Online service)
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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
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Technological Retardation
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No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
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Lymphedema
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
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Technological Retardation
Drivers of cost differences between US breast cancer survivors with or without lymphedema
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