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Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)

The Lujan-Fryns syndrome or X-linked mental retardation with marfanoid habitus syndrome is a syndromal X-linked form of mental retardation, affecting predominantly males. The prevalence is not known for the general population. The syndrome is associated with mild to moderate mental retardation, dist...

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Detalles Bibliográficos
Autores principales: Van Buggenhout, Griet, Fryns, Jean-Pierre
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538574/
https://www.ncbi.nlm.nih.gov/pubmed/16831221
http://dx.doi.org/10.1186/1750-1172-1-26
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author Van Buggenhout, Griet
Fryns, Jean-Pierre
author_facet Van Buggenhout, Griet
Fryns, Jean-Pierre
author_sort Van Buggenhout, Griet
collection PubMed
description The Lujan-Fryns syndrome or X-linked mental retardation with marfanoid habitus syndrome is a syndromal X-linked form of mental retardation, affecting predominantly males. The prevalence is not known for the general population. The syndrome is associated with mild to moderate mental retardation, distinct facial dysmorphism (long narrow face, maxillary hypoplasia, small mandible and prominent forehead), tall marfanoid stature and long slender extremities, and behavioural problems. The genetic defect is not known. The diagnosis is based on the presence of the clinical manifestations. Genetic counselling is according to X-linked recessive inheritance. Prenatal testing is not possible. There is no specific treatment for this condition. Patients need special education and psychological follow-up, and attention should be given to diagnose early psychiatric disorders.
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spelling pubmed-15385742006-08-10 Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus) Van Buggenhout, Griet Fryns, Jean-Pierre Orphanet J Rare Dis Review The Lujan-Fryns syndrome or X-linked mental retardation with marfanoid habitus syndrome is a syndromal X-linked form of mental retardation, affecting predominantly males. The prevalence is not known for the general population. The syndrome is associated with mild to moderate mental retardation, distinct facial dysmorphism (long narrow face, maxillary hypoplasia, small mandible and prominent forehead), tall marfanoid stature and long slender extremities, and behavioural problems. The genetic defect is not known. The diagnosis is based on the presence of the clinical manifestations. Genetic counselling is according to X-linked recessive inheritance. Prenatal testing is not possible. There is no specific treatment for this condition. Patients need special education and psychological follow-up, and attention should be given to diagnose early psychiatric disorders. BioMed Central 2006-07-10 /pmc/articles/PMC1538574/ /pubmed/16831221 http://dx.doi.org/10.1186/1750-1172-1-26 Text en Copyright © 2006 Van Buggenhout and Fryns; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Van Buggenhout, Griet
Fryns, Jean-Pierre
Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
title Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
title_full Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
title_fullStr Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
title_full_unstemmed Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
title_short Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
title_sort lujan-fryns syndrome (mental retardation, x-linked, marfanoid habitus)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1538574/
https://www.ncbi.nlm.nih.gov/pubmed/16831221
http://dx.doi.org/10.1186/1750-1172-1-26
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