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

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