Gene Found For Rare Disorder May Reveal New Pathway In Mental Retardation
Tue, 20 Feb 2007 04:00 AM EST
... Studying mutations that give rise to a rare genetic disease, genetics researchers have identified a novel biological pathway that may have a broader role during human development, potentially in cases of mental retardation and autism. An international team of researchers identified two genes that contribute to Cornelia deLange syndrome, a multisystem genetic disease that affects an estimated one in 10,000 children. ...
Related Topics
- Mental Retardation
- Blood Disorders
- Mental Health
- Rare Diseases
- Child Mental Health
- Genetic Disorders
- Adrenal Gland Disorders
- Developmental Disabilities & Disorders
- Developmental Disabilities
- Muscle Disorders
- Emotional Disorders
- Genes and Gene Therapy
- Sleep Disorders
- Borderline Personality Disorder
- Coffin Lowry Syndrome
- Communication Disorders
- Dissociative Disorders
- Seizure Disorder
- Language Disorders
- Seasonal Affective Disorder

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