Feingold syndrome

Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold, an American physician who first described the syndrome in 1975. Until 2003, at least 79 patients have been reported worldwide.[1]

Feingold syndrome
Other namesOculodigitoesophagoduodenal syndrome
Feingold Syndrome is inherited in an autosomal dominant fashion.
SpecialtyMedical genetics 

Presentation

Feingold syndrome is marked by various combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and sometimes learning disability or mental retardation.[2]

Genetics

Feingold syndrome is caused by mutations in the neuroblastoma-derived V-myc avian myelocytomatosis viral-related oncogene (MYCN) which is located on the short arm of chromosome 2 (2p24.1). This syndrome has also been linked to microdeletions in the MIR17HG locus which encodes a micro RNA cluster known as miR-17/92.[3]

Diagnosis

The diagnosis is based on the following clinical findings:

Treatment

There is no known treatment for the disorder, but surgery for malformations, special education, and treatment of hearing loss are important.[4]

gollark: I should probably trade with sun for a gold but I'm not patient/reliable enough for IOUs.
gollark: They're just ridiculously somethingful.
gollark: I mean, likely you won't be *banned*, but I also expect they'll do *nothing about this*.
gollark: Ah, but we must remember that these are *DC* moderators.
gollark: They'll probably just say "IOUs are not our problem hahahahahahahaha".

References
  1. Tészás A, Meijer R, Scheffer H, et al. (October 2006). "Expanding the clinical spectrum of MYCN-related Feingold syndrome". Am. J. Med. Genet. A. 140 (20): 2254–6. doi:10.1002/ajmg.a.31407. PMID 16906565.
  2. Celli J, van Bokhoven H, Brunner HG (November 2003). "Feingold syndrome: clinical review and genetic mapping". Am. J. Med. Genet. A. 122A (4): 294–300. doi:10.1002/ajmg.a.20471. PMID 14518066.
  3. Marcelis, Carlo L. M.; Hol, Frans A.; Graham, Gail E.; Rieu, Paul N. M. A.; Kellermayer, Richard; Meijer, Rowdy P. P.; Lugtenberg, Dorien; Scheffer, Hans; Bokhoven, Hans van (2008). "Genotype–phenotype correlations in MYCN-related Feingold syndrome". Human Mutation. 29 (9): 1125–1132. doi:10.1002/humu.20750. ISSN 1098-1004.
  4. "Feingold Syndrome 1 | Hereditary Ocular Diseases". disorders.eyes.arizona.edu. Retrieved 2019-10-07.
Classification
External resources
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