Medicine:Cataract-microcornea syndrome

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Cataract-microcornea syndrome
Other namesMicrocornea cataract syndrome[1]
Autosomal dominant - en.svg
Cataract-microcornea syndrome is inherited in an autosomal dominant manner[2]

The cataract-microcornea syndrome is the association of congenital cataract and microcornea.

Genetics

Mutations in ABCA3 were found to be associated to this syndrome.[3]

Diagnosis

Treatment

References

  1. "Cataract microcornea syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". https://rarediseases.info.nih.gov/diseases/1155/index. Retrieved 18 October 2019. 
  2. "OMIM Entry - # 116200 - CATARACT 1, MULTIPLE TYPES; CTRCT1" (in en-us). https://omim.org/entry/116200. Retrieved 1 September 2017. 
  3. Chen, P; Dai, Y; Wu, X; Wang, Y; Sun, S; Xiao, J; Zhang, Q; Guan, L et al. (2014). "Mutations in the ABCA3 gene are associated with cataract-microcornea syndrome". Investigative Ophthalmology & Visual Science 55 (12): 8031–43. doi:10.1167/iovs.14-14098. PMID 25406294. 

External links

Classification
External resources