Intellectual Disability
|
0.500 |
Biomarker
|
group |
HPO |
|
|
|
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Only recently have mutations in MECP2 been found to be a cause of Rett Syndrome (RTT), a neuro-developmental disorder characterized by mental retardation, loss of expressive speech, deceleration of head growth and loss of acquired skills that almost exclusively affects females.
|
10814718 |
2000 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
CLINVAR |
Chronic osteomyelitis in patients with sickle cell disease.
|
10944834 |
2000 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Consistent with this notion is the recent demonstration that MECP2 mutations cause Rett syndrome (RTT, MIM 312750), a childhood neurological disorder that represents one of the most common causes of mental retardation in females.
|
11242118 |
2001 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
Therefore, implementation of systematic screening of MECP2 in MR patients should result in significant progress in the field of molecular diagnosis and genetic counseling of mental handicap.
|
11309367 |
2001 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
The authors recently described a novel A140V MECP2 missense mutation in an Italian family with X-linked semidominant mental retardation.
|
11805248 |
2002 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
To date, descriptions have been published of two patients with independent familial mental retardation (MR) and two patients with sporadic MR who harbor this specific mutation in the MECP2 gene.
|
11885030 |
2002 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Numerous recent reports have proposed that mutations in the C-terminal domain of the MECP2 gene could be a frequent cause of mental retardation in males.
|
11896461 |
2002 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
This case, as well as other published studies of males with MECP2 mutations, reveals that the clinical manifestations in viable males vary from neonates with severe encephalopathy to adults with mental retardation and demonstrate genotype-phenotype correlations.
|
11913564 |
2002 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
CLINVAR |
Prenatal diagnosis in Rett syndrome.
|
12065946 |
2003 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
|
12325019 |
2002 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Most male patients with MeCP2 mutations exhibit moderate to severe developmental delay/mental retardation.
|
12555243 |
2003 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
Recently, mutations in the MECP2 gene were reported in males with non-specific mental retardation suggesting that defects in MECP2 could be responsible for up to 2% of X-linked mental retardation.
|
14529314 |
2003 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
In this study, the question was addressed as to whether implementation of systematic screening of MECP2 in patients with an unexplained mental retardation in DNA diagnostics would be reasonable, and the spectrum of phenotypes resulting from mutations in this gene was further explored.
|
14560307 |
2004 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Rett syndrome (RTT), the second most common cause of mental retardation in females, has been associated with mutations in MeCP2, the archetypical member of the methyl-CpG binding domain (MBD) family of proteins.
|
15549394 |
2005 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Macrocephalic mental retardation associated with a novel C-terminal MECP2 frameshift deletion.
|
15558314 |
2005 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
The aim of this study was to analyze well-characterized cases with MR and to clarify the role of the MECP2 gene in the etiology of MR and atypical Angelman syndrome.
|
15578581 |
2005 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
MECP2 gene mutations responsible for Rett syndrome have also been found in male patients with mental retardation, sometimes associated with different neurologic abnormalities.
|
15704871 |
2004 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
We consider essential proceeding further screening in the whole extension of the MECP2 gene using clinically well-documented and larger sized sample to assure the overall contribution of MECP2 to mental retardation.
|
15814190 |
2005 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
Comparison of the clinical features in these patients and in a previously reported patient enables refinement of the genotype-phenotype correlation and strongly suggests that increased dosage of MECP2 results in the MR phenotype.
|
16080119 |
2005 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
LHGDN |
Comparison of the clinical features in these patients and in a previously reported patient enables refinement of the genotype-phenotype correlation and strongly suggests that increased dosage of MECP2 results in the MR phenotype.
|
16080119 |
2005 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
The phenotypic spectrum of MECP2 mutations is broad and includes mental retardation with or without seizures, Angelman syndrome-like phenotype, and autism.
|
16225828 |
2005 |
Intellectual Disability
|
0.500 |
Biomarker
|
group |
BEFREE |
Based on the literature, MECP2 testing in males with MR only is debatable.
|
16376510 |
2006 |
Intellectual Disability
|
0.500 |
AlteredExpression
|
group |
BEFREE |
The need for tightly controlled MeCP2 levels in brain is strongly suggested by neurologically abnormal phenotypes of mouse models with mild overexpression and by mental retardation in human males with MECP2 duplication.
|
16613900 |
2006 |
Intellectual Disability
|
0.500 |
GeneticVariation
|
group |
BEFREE |
Rett syndrome, a neurodevelopmental disorder caused by mutations in the X-linked gene encoding methyl-CpG-binding protein 2 (MeCP2), is a leading cause of mental retardation with autistic features in females.
|
16647848 |
2006 |