MGZ Medizinisch Genetisches Zentrum

X-Linked Mental Retardation, XLMR

Klinische Symptomatik

A prevalence of approximately 3% is reported for mental retardation. In about 25 to 35%, mental retardation is caused by genetic defects. Among them, most (5 – 18%) of the cases are caused by X-linked mental retardation which preferably affects males and which is caused by the fragile X syndrome in 15 to 20%. In the remainder of cases, syndromic and non-syndromic forms of X-linked retardation are known. Typical dysmorphic features are found in all affected family members in the syndromic forms. Family members affected by the non-syndromic forms do not show further dysmorphic features or neurological symptoms besides mental retardation. X-linked mental retardation should be considered if, consistent with X-linked inheritance, at least two family members are affected. The diagnostic procedures have to be discussed individually.

Genetik

X-linked mental retardation is caused by a large number of different genetic defects on the X chromosome.

Häufigkeit

1 : 500 in men

 

Diagnostik

 

Indikation

Mental retardation of unknown origin in male family members, related to each other via the female line. 

Methodik

Linkage analysis using polymorphic microsatellite markers on the X chromosome. Blood samples of as many affected and non-affected family members as possible are required.

Material

2 - 4 ml of EDTA blood

Dauer

Depending on family size, upon agreement

Versand

Mail at room temperature or laboratory courier

Beratung

For genetic counselling please call ++49-89-3090 886-0





MGZ
Medizinisch Genetisches Zentrum

Bayerstraße 3-5 (durch die Mathäser-Passage)

Eingang Schlosserstraße 6
80335 München
info@mgz-muenchen.de
Tel. +49 (0)89/30 90 886-0
Fax +49 (0)89/30 90 886-66

Ärztliche Leitung
Prof. Dr. med. Dipl. chem. Elke Holinski-Feder