X-LINKED INTELLECTUAL DISABILITY

被引：0

作者：

Maria, Piccione ^{[1
]}

Antona, Vincenzo ^{[1
]}

Graziano, Luciano ^{[1
]}

Consiglio, Valeria ^{[2
]}

Salzano, Emanuela ^{[1
]}

Vecchio, Davide ^{[1
]}

Lauricella, Salvatrice Antonia ^{[3
]}

Corsello, Giovanni ^{[1
]}

机构：

[1] Univ Palermo, Dipartimento Sci Promoz Salute & Materno Infantil, I-90133 Palermo, Italy

[2] CRR Malattie Rare AOOR Villa Sofia Cervello Paler, Palermo, Italy

[3] Lab Citogenet Med AOOR Villa Sofia Cervello Paler, Palermo, Italy

来源：

ACTA MEDICA MEDITERRANEA | 2013年 / 29卷 / 04期

关键词：

intellectual disability X-linked; syndromic forms; dysmorphic features; SENSORINEURAL HEARING-LOSS; COPY NUMBER VARIATIONS; MENTAL-RETARDATION; EXPRESSIVE LANGUAGE; RISK-FACTORS; ADOLESCENTS; PROFILES; ETIOLOGY; EPILEPSY;

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

The intellectual disability is found in approximately 2-3% of the population in a mild-to-moderate form and 0.5-1% in a moderate-to-severe form. The mutations on the chromosome X are responsible for both syndromic and non-syndromic intellectual disability. In the syndromic forms behavioral disorders, autism and/or seizures are frequent.

引用

页码：799 / 802

页数：4

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