Jung syndrome
A rare congenital malformation syndrome characterized by the association of anterior ocular chamber cleavage disorder with developmental delay short stature and congenital hypothyroidism. Additional manifestations include cerebellar hypoplasia tracheal stenosis narrow external auditory meatus and hip dislocation. There have been no further description in the literature since 1995.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.
Newly diagnosed with
Jung syndrome?
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Advocacy Organizations
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
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