Joubert’s Syndrome: A Case Report.

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dc.contributor.authorAmin, A
dc.contributor.authorFarooq, A
dc.contributor.authorAli, M Lone
dc.contributor.authorIrfan, H
dc.contributor.authorWani, S
dc.contributor.authorHamid, R
dc.date.accessioned2013-07-09T09:34:27Z
dc.date.available2013-07-09T09:34:27Z
dc.date.issued2011-05
dc.description.abstractJoubert’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.en_US
dc.identifier.citationAmin A, Farooq A, Ali M Lone, Irfan H, Wani S, Hamid R. Joubert’s Syndrome: A Case Report. Journal of Nepal Paediatric Society. 2011 May-Aug; 31(2): 141-142.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/147174
dc.language.isoenen_US
dc.source.urihttps://www.nepjol.info/index.php/JNPS/article/view/3908/3857en_US
dc.subjectJoubert’s syndromeen_US
dc.subjectmolar tooth signen_US
dc.subjectcerebellar pedunclesen_US
dc.subjectvermis hypoplasiaen_US
dc.titleJoubert’s Syndrome: A Case Report.en_US
dc.typeArticleen_US
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