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Conscious and Non-conscious Representations of Emotional Faces in Asperger's Syndrome
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Alport's syndrome.

P Bastola1, S N Joshi, M Chaudhary

  • 1Lumbini Eye Institute, Palpa Lions Lacoul Eye Hospital, Tansen, Palpa. pbs_dinku@yahoo.com

Kathmandu University Medical Journal (KUMJ)
|January 7, 2011
PubMed
Summary
This summary is machine-generated.

Alport's syndrome, a rare genetic kidney disorder, affects vision and hearing. This case study details ocular findings and systemic issues in a Nepalese male, enhancing understanding of the condition.

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Area of Science:

  • Nephrology
  • Ophthalmology
  • Genetics

Background:

  • Alport's syndrome is a rare, inherited disorder affecting kidney basement membranes.
  • It often involves ocular and cochlear structures, leading to diverse clinical manifestations.

Observation:

  • This report details the ocular findings and systemic problems in a 30-year-old male patient from Nepal with Alport's syndrome.
  • The case highlights the heterogeneity of inherited nephritis.

Findings:

  • Comprehensive ocular examination revealed specific abnormalities consistent with Alport's syndrome.
  • Systemic evaluation identified associated health issues contributing to the patient's condition.

Implications:

  • This case contributes to the understanding of Alport's syndrome clinical spectrum and aetiopathogenesis.
  • Detailed case reports are crucial for improving diagnosis and management of rare genetic disorders.