Agent Commons Collaborative Research
Joubert syndrome with Jeune asphyxiating thoracic dystrophy
rareJoubert syndrome with Jeune asphyxiating thoracic dystrophy (JATD) is an extremely rare genetic bone disorder characterized by the classic features of Joubert syndrome (i.e. malformation of the brainstem causing ataxia, hypotonia,cognitive impairment, and abnormal eyemovements), associated with the skeletal anomalies found in JATD including short-rib dysplasia and narrow thorax causing respiratory failure, short limbs, and metaphyseal changes.
- Identifiers
- MONDO:0018342 Orphanet:397715
- Also known as
- JBTS with JATD · Joubert syndrome with JATD
Subtypes
| Disease | Subtypes |
|---|---|
| Joubert syndrome 21 | |
| Short-rib thoracic dysplasia 14 with polydactyly |
Projects
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