Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)
نویسندگان
چکیده
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.
منابع مشابه
X-linked mental retardation with marfanoid habitus.
Here we report on two pairs of mildly to moderately mentally retarded brothers with marfanoid habitus and similar craniofacial changes. They had a long and narrow face, small mandible, high-arched palate, and hypernasal voice, as previously reported by Lujan et al (Am J Med Genet 17:311-322, 1984) in four mentally retarded males of a large kindred. The present data suggest the existence of a sp...
متن کاملLujan–Fryns Syndrome (LFS): A Unique Combination of Hypernasality, Marfanoid Body Habitus, and Neuropsychiatric Issues, Presenting as Acute-Onset Dysphagia
BACKGROUND Lujan-Fryns syndrome (LFS) is an extremely rare, X-linked disorder, for which the full clinical spectrum is still unknown. Usually, it presents with neuropsychiatric problems such as learning disabilities and behavioral issues in a typical combination with marfanoid features. Often, there is a positive family history for the disorder. However, sporadic cases have also been reported i...
متن کاملTentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities?
The clinical diagnosis of Lujan-Fryns syndrome (LFS) comprises X-linked intellectual disability (XLID) with marfanoid habitus, distinct combination of minor facial anomalies and nasal speech. However the definition of syndrome was significantly broadened since the original report and implies ID with marfanoid habitus. Mutations of three genes (MED12, UPF3B, and ZDHHC9) have been reported in "br...
متن کاملMarfanoid features and X-linked mental retardation associated with craniofacial abnormalities: the Lujan-Fryns syndrome Aspectos marfanoides e retardo mental ligado ao X associados a anormalidades craniofaciais: síndrome de Lujan-Fryns
Appleton1, in 1911, reported the first description of this anatomical variation based on a forearm dissection. He found only the posterior radial nerve interosseous branch with absent SRN, below the elbow. On the dorsum of the hand, the LACN extended out beyond its usual distribution to supply the SRN territory (Figure). The dorsal branch of the ulnar nerve had greater ramifications than those ...
متن کاملLETTER TO JMG Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation
T Kleefstra, H G Yntema, A R Oudakker, M J G Banning, V M Kalscheuer, J Chelly, C Moraine, H-H Ropers, J-P Fryns, I M Janssen, E A Sistermans, W N Nillesen, L B A de Vries, B C J Hamel, H van Bokhoven . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ...
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ورودعنوان ژورنال:
- Orphanet Journal of Rare Diseases
دوره 1 شماره
صفحات -
تاریخ انتشار 2006