2 Congenital Fibrosis Of Extraocular Muscles

mutation in ARIX

Also Known As:

Fibrosis Of Extraocular Muscles, Congenital, 2; CFEOM2; Fibrosis Of Extraocular Muscles, Congenital, Autosomal Recessive

Networked: 4 relevant articles (0 outcomes, 0 trials/studies)

1.	Strabismus (Squint)
2.	Low Vision (Subnormal Vision)
3.	Fibrosis (Cirrhosis)
4.	congenital fibrosis of the extraocular muscles

1.	Engle, Elizabeth C: 3 articles (01/2016 - 11/2003)
2.	Abu-Amero, Khaled: 2 articles (01/2016 - 09/2006)
3.	Oystreck, Darren T: 2 articles (01/2016 - 09/2006)
4.	Ghalla, Pooja: 1 article (10/2017)
5.	Matalia, Jyoti Himanshu: 1 article (10/2017)
6.	Panmand, Pratibha: 1 article (10/2017)
7.	Almutlaq, Mohammed: 1 article (01/2016)
8.	Bosley, Thomas: 1 article (01/2016)
9.	Khan, Arif O: 1 article (01/2016)
10.	Bosley, Thomas M: 1 article (09/2006)

Drugs and Important Biological Agents (IBA) related to 2 Congenital Fibrosis Of Extraocular Muscles:

1.	Nonsense Codon (Nonsense Mutation)IBA 11/01/2003 - "This is the fourth CFEOM2 mutation in PHOX2A and the first nonsense mutation to be identified. "
2.	Transcription Factors (Transcription Factor)IBA 09/01/2006 - "Congenital fibrosis of the extraocular muscles type 2 (CFEOM2) is a complex strabismus syndrome that results from mutations in the homeodomain transcription factor PHOX2A. "
3.	Retinaldehyde (Retinal)IBA 01/01/2016 - "In addition to a distinct form of congenital incomitant strabismus, the phenotype of CFEOM2 includes subnormal vision consistent with retinal dysfunction. "

1.	Sutures (Suture) 10/01/2017 - "He was diagnosed with congenital fibrosis of extraocular muscles, type 2 (CFEOM2) and operated upon in a staged procedure with a satisfactory eye alignment using hang-back sutures in one eye and periosteal fixation in the other. "