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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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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. |
format | Text |
id | pubmed-1538574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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