Conductive deafness-ptosis-skeletal anomalies syndrome
| Conductive deafness-ptosis-skeletal anomalies syndrome | |
|---|---|
| Other names | Jackson Barr syndrome |
 | |
| Deaths | - |
Conductive deafness-ptosis-skeletal anomalies syndrome, also known as Jackson Barr syndrome,[1] is a rare presumably autosomal recessive genetic disorder characterized by conductive hearing loss associated with external auditory canal-middle ear atresia which aggravates during ear infections, ptosis, and skeletal anomalies which consist of clinodactyly of the fifth fingers, radial head dislocation and internal rotation of the hips).[2][3] Additional findings include thin nose, hair growth delays, and teeth dysplasia.[4] It has been described in two American sisters.[5]
References
[edit]- ^ Roberts, Sean (16 June 2022). "Deafness conductive ptosis skeletal anomalies". NORD (National Organization for Rare Disorders). Retrieved 2022-08-11.
- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Conductive deafness ptosis skeletal anomalies syndrome". www.orpha.net. Retrieved 2022-08-11.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ "Conductive Deafness-Ptosis-Skeletal Anomalies Syndrome". DoveMed. Retrieved 2022-08-11.
- ^ "Deafness conductive ptosis skeletal anomalies - About the Disease - Genetic and Rare Diseases Information Center". rarediseases.info.nih.gov. Retrieved 2022-08-11.
- ^ "Entry - 221320 - DEAFNESS, CONDUCTIVE, WITH PTOSIS AND SKELETAL ANOMALIES - OMIM". omim.org. Retrieved 2022-08-11.
 | This genetic disorder article is a stub. You can help Wikipedia by expanding it. |