Kindler′s syndrome: A case series of three Indian children
نویسندگان
چکیده
منابع مشابه
joubert syndrome in three children in a family: a case series
abstract how to cite this article: akhondian j, ashrafzadeh f, beiraghi toosi m, moazen n, mohammadpoor t, karimi r. joubert syndrome in three children in a family: a case series. iran j child neurol. 2013 winter: 7(1); 39-42. joubert syndrome (js) is a rare autosomal recessive central nervous system malformation characterized by hypoplasia of the cerebellar vermis, hypotonia and abn...
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Joubert syndrome (JS) is a rare autosomal recessive central nervous system malformation characterized by hypoplasia of the cerebellar vermis, hypotonia and abnormal psychomotor development, along with altered respiratory pattern and various ophthalmologic features. Here, we describe three children with Joubert syndrome in a family that had almost similar presentations, including ataxia, develop...
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ژورنال
عنوان ژورنال: Indian Journal of Dermatology
سال: 2010
ISSN: 0019-5154
DOI: 10.4103/0019-5154.74568