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Related Experiment Videos

Carney complex.

Rayhaneh G Zahedi1, David S Wald, Sunil Ohri

  • 1Southampton University Hospital, Southampton, Hampshire, United Kingdom.

The Annals of Thoracic Surgery
|June 27, 2006
PubMed
Summary
This summary is machine-generated.

Carney complex, a rare genetic disorder, typically presents earlier. This case highlights a 61-year-old woman with multiple atrial myxomas and skin pigmentation, emphasizing lifelong screening for affected families.

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Area of Science:

  • Cardiology
  • Genetics
  • Dermatology

Background:

  • Carney complex is a rare genetic disorder characterized by spotty skin pigmentation and myxoma tumors.
  • It typically manifests in childhood or early adulthood, with a median age of onset around 20 years.

Observation:

  • This report details an unusual case of Carney complex presenting at age 61.
  • The patient exhibited multiple atrial myxomas and cutaneous hyperpigmentation.
  • A significant family history of atrial myxomas and sudden cardiac death was noted.

Findings:

  • The late presentation in this case challenges typical Carney complex timelines.
  • Genetic predisposition and familial clustering of cardiac myxomas are evident.

Implications:

Related Experiment Videos

  • Highlights the need for lifelong echocardiographic screening and surveillance in all family members of Carney complex patients.
  • Emphasizes considering Carney complex in older individuals with unexplained cardiac myxomas and pigmentation.
  • Underscores the importance of family history in diagnosing and managing rare genetic syndromes.