Browsing by Author "Ali, M Lone"

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    Joubert’s Syndrome: A Case Report.
    (2011-05) Amin, A; Farooq, A; Ali, M Lone; Irfan, H; Wani, S; Hamid, R
    Joubert’s syndrome is an autosomal recessive congenital disorder having characteristic clinical features like hypotonia, ataxia, developmental delay and many neurological problems. Other variable features include retinal dystrophy, cystic kidney disease liver fibrosis etc. Treatment for Joubert syndrome is symptomatic and supportive. Infant stimulation and physical, occupational, and speech therapy may benefit some patients. Infants with abnormal breathing patterns should be monitored.