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ALLMedicine™ Ablepharon Macrostomia Syndrome Center

Research & Reviews  7 results

A case of ablepharon macrostomia syndrome requiring multidisciplinary care.
https://doi.org/10.1080/08164622.2021.1878839
Clinical & Experimental Optometry; Alexopoulos D, Matchinski TL

Mar 10th, 2021 - A case of ablepharon macrostomia syndrome requiring multidisciplinary care.|2021|Alexopoulos D,Matchinski TL,|

Ablepharon Macrostomia Syndrome: Rib Cartilage and Fat Grafting for Lower Lid Reconstru...
https://doi.org/10.1097/SCS.0000000000007187
The Journal of Craniofacial Surgery; Kurnik NM, Leach GA et. al.

Oct 15th, 2020 - Ablepharon macrostomia syndrome (AMS) is a rare condition with fewer than 20 cases being reported in the literature. Features of AMS include ablepharon, hypertelorism, macrostomia, dysplastic ears, sparse body hair, and ambiguous genitalia. The mo...

Laryngo-tracheal stenosis in a woman with ablepharon macrostomia syndrome.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712709
BMC Pulmonary Medicine; Ciriaco P, Carretta A et. al.

Aug 29th, 2019 - Ablepharon macrostomia syndrome (AMS) is a rare congenital malformation disorder caused by the autosomal-dominant mutations in gene TWIST2. Patients affected by the disease present abnormalities in ectoderm-derived structures mainly consisting in ...

Ablepharon macrostomia syndrome
https://rarediseases.info.nih.gov/diseases/3/ablepharon-macrostomia-syndrome

Mar 5th, 2017 - Ablepharon macrostomia syndrome is genetic disorder characterized by absent eyelids (ablepharon) and very large mouth (macrostomia). Other common signs and symptoms include abnormal external ears, fusion (syndactyly) of the hands and feet, skin fi...

Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barb...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4572501
American Journal of Human Genetics; Marchegiani S, Davis T et. al.

Jun 29th, 2015 - Ablepharon macrostomia syndrome (AMS) and Barber-Say syndrome (BSS) are rare congenital ectodermal dysplasias characterized by similar clinical features. To establish the genetic basis of AMS and BSS, we performed extensive clinical phenotyping, w...

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