Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)- the new lacunae: a case report
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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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
- Creator
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Silva, Nuno Álvaro
Silva, Renato Emílio Santos
Magalhães, António Augusto
- Contributor
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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
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:22 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Silva, Nuno Álvaro
- Silva, Renato Emílio Santos
- Magalhães, António Augusto
- SpringerLink (Online service)
Other Objects (12)
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
Central Serous Chorioretinopathy Associated with Desmopressin Nasal Spray: Causality or Unfortunate Association
Lymphedema
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Mental retardation
Technological Retardation
Drivers of cost differences between US breast cancer survivors with or without lymphedema
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration
Intrauterine growth retardation
The relationship between lymphedema severity and awareness of lymphedema surgery
Brachytherapy for Central Serous Chorioretinopathy
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
Central Serous Chorioretinopathy Associated with Desmopressin Nasal Spray: Causality or Unfortunate Association
Lymphedema
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Mental retardation
Technological Retardation
Drivers of cost differences between US breast cancer survivors with or without lymphedema
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration
Intrauterine growth retardation
The relationship between lymphedema severity and awareness of lymphedema surgery
Brachytherapy for Central Serous Chorioretinopathy
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
Central Serous Chorioretinopathy Associated with Desmopressin Nasal Spray: Causality or Unfortunate Association
Lymphedema
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Mental retardation
Technological Retardation
Drivers of cost differences between US breast cancer survivors with or without lymphedema
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation
The supposed tumor suppressor gene WWOX is mutated in an early lethal microcephaly syndrome with epilepsy, growth retardation and retinal degeneration
Intrauterine growth retardation
The relationship between lymphedema severity and awareness of lymphedema surgery