Autism Spectrum Disorders and Oculocutaneous Albinism - A Case Report in Indian Scenario

Authors

  • Sandhya* Lecturer in Speech Language Pathology, JSS Institute of Speech and Hearing, India Author
  • Aravinda HR Clinical Supervisor, Grade I at JSS Institute of Speech and Hearing, India Author

DOI:

https://doi.org/10.23880/PNBOA-16000123

Keywords:

Oculocutaneous albinism, Autistic spectrum disorder, Skin disorders

Abstract

Oculocutaneous albinism (OCA) is a collection of autosomal recessive condition of melanin biosynthesis that rarely presents with multiple systemic exhibitions. This article accounts a case of co-morbid childhood autism and Oculocutaneous albinism in a 4 years old girl from Hubli, a city in North Karnataka region of India. The proposed case presentation is a documentation of rare condition where OCA is associated with Albinism. A Detailed Speech language profile based on systematic evaluation has been highlighted in the present study.

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Published

2025-08-12

Issue

Vol. 3 No. 3 (2018)

Section

Articles

License

Copyright (c) 2018 Sandhya

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.

How to Cite

Autism Spectrum Disorders and Oculocutaneous Albinism - A Case Report in Indian Scenario . (2025). Pediatrics & Neonatal Biology Open Access, 3(3), 1-3. https://doi.org/10.23880/PNBOA-16000123

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