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Angelman Syndrome: Multidisciplinary Management.

Whitney A Bridges1, Heide S Temples2, Tracy B Lowe3

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Summary
This summary is machine-generated.

Angelman syndrome is a rare genetic disorder caused by the loss of the maternal UBE3A gene. Early identification and multidisciplinary care are crucial for managing developmental delays and improving outcomes for affected infants.

Keywords:
Angelman SyndromeUBE3A geneneurodevelopmental disorder

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Area of Science:

  • Genetics
  • Developmental Pediatrics
  • Rare Diseases

Background:

  • Angelman syndrome is a rare genetic disorder characterized by genomic imprinting and the loss of the maternal UBE3A gene.
  • It presents with diverse phenotypes, including significant developmental delays.
  • Current management focuses on supportive and symptomatic treatment due to the absence of a cure.

Purpose of the Study:

  • To review the clinical presentation of Angelman syndrome for early infant identification.
  • To outline diagnostic criteria and management strategies.
  • To discuss family resources, primary care implications, and future therapeutic avenues.

Main Methods:

  • Case presentation of a nine-month-old diagnosed with Angelman syndrome.
  • Review of clinical manifestations, diagnostic criteria, and treatment approaches.
  • Exploration of multidisciplinary care requirements and emerging therapies.

Main Results:

  • The case highlights the importance of recognizing developmental delays for early diagnosis.
  • Genetic testing confirmed Angelman syndrome.
  • A multidisciplinary approach is essential for comprehensive patient care.

Conclusions:

  • Early identification of Angelman syndrome in infants is critical for timely intervention.
  • A coordinated, multidisciplinary approach is necessary for optimal management.
  • Ongoing research into future therapies offers hope for improved outcomes.