Results 81 to 90 of about 1,431,497 (181)

Successful surgical management of bilateral incomplete cryptophthalmos: A stitch in time

Journal of Clinical Ophthalmology and Research
We report the clinical features and management of a 22-day-old male infant with bilateral incomplete cryptophthalmos, born of consanguineous marriage. Examination revealed upper lid colobomas, symblepharon with superior cornea, and obliterated fornices ...
Purvasha Narang, Milind N Naik, Muralidhar Ramappa   +2 more
doaj   +1 more source

Fraser of cryptophthalmosis syndrome: A case report [PDF]

, 2004
Fraser or cryptophthalmos syndrome is a rare autosomal recessive disorder characterized by major features such as cryptophthalmos, syndactyly, and abnormal genitalia. Consanguinity is reported in 15-24.8% of the cases.
Haidary, K., Khoury, E., Adibi, B., Golalipour, M.-J.   +3 more
core  

Comprehensive analysis of Fraser syndrome 1 as a potential biomarker and therapeutic target in hepatocellular carcinoma

Journal of Radiation Research and Applied Sciences
Background: Fraser syndrome 1 (FRAS1) is an extracellular matrix (ECM) protein that plays a vital role in epidermal basement membrane adhesion and organ development. FRAS1 also plays a crucial role in cancer development.
Zeyu Sun, Chaoxin Jin, Xuanchen Tao, Pengge Wang, Baiying Liu, Xinyu Xing, Tiewei Sun   +6 more
doaj   +1 more source

A Rare Case of Fraser Syndrome with Partial Vaginal Agenesis and Its Successful Reconstructive Cosmetic Management: A Case Report. [PDF]

J Obstet Gynaecol India, 2022
Panigrahi S, Mohapatra K, Pradhan M, Mishra S, Samal S.   +4 more
europepmc   +1 more source

Eyelid and Fornix Reconstruction in Bilateral Abortive Cryptophthalmos (Fraser Syndrome)

, 1992
Cryptophthalmos refers to a group of uncommon congenital anomalies of eyelid formation that can occur alone or in combination with multiple congenital anomalies as part of the Fraser syndrome.
Clarke, MP, Rootman, DS, Sullivan, TJ, Pashby, RC   +3 more
core   +1 more source

Fraser syndrome [PDF]

, 2020
openaire   +3 more sources

FRASER SYNDROME [PDF]

, 2018
Methodius G. Tuuli, Anthony O. Odibo
openaire   +2 more sources

Recurrent abdominal pain as a leading symptom for branchio-oto-renal syndrome: a case report

Journal of Medical Case Reports
Background Branchio-oto-renal syndrome is a rare autosomal dominant disorder characterized by hearing impairment, branchial arch anomalies, preauricular pits, and renal malformations.
Alaa Senjab, Omar Al Ayoubi, Grace Tannous, Yaman Alsharef   +3 more
doaj   +1 more source

Sir Simon Fraser at the Fraser family house at Oban, Scotland.

, 1911
This record was harvested from a previous catalogue system and will be withdrawn in 2025. Information in this record may be superseded or incomplete.
Fraser, John N.
core  

Prenatal diagnosis of Fraser syndrome caused by novel variants of FREM2. [PDF]

Hum Genome Var, 2020
Ikeda S, Akamatsu C, Ijuin A, Nagashima A, Sasaki M, Mochizuki A, Nagase H, Enomoto Y, Kuroda Y, Kurosawa K, Ishikawa H.   +10 more
europepmc   +1 more source