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Prader Willi and Angelman Syndrome

Prader Willi and Angelman Syndrome

Company Name / Date

Uniparental Diseases

Uniparental Dieases

Treatment

Common Causes 

Phenotype

Mainly Supportive Therapies

Possible Medications to help with side effects

Mutations in UBE3A

Maternal Deletions

Parental Uniparental Disomy

Imprinting defects on 15q11-q13

Happy Disposition

Sezuires

Ataxia 

Angelman Syndrome

Prader Willi Syndrome

Phenotype

Common Causes

Treatment

Obese

Mental Retardation

Light skin and eyes

Deletion

Genomic Imprinting

Maternal Uniparental Disomy

Replacement therapies

Diet management

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publish time: 2021-03-24
WSDec6l7

This mind map shows the Angelman syndrome and Prader Willi. Prader-Willi (PWS) and Angelman (AS) syndromes are two rare genetic disorders caused by imprinting defects in the same region of chromosome 15. From this mind map, it analyzes its symptom,type and research. Want to learn more about Prader Willi and Angelman Syndrome, click this mind map. Or you may use the mind map to visualize your knowledge with ease.

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