|1.||Knoepfler, Paul S: 2 articles (12/2010 - 06/2010)|
|2.||Wey, Alice: 2 articles (12/2010 - 06/2010)|
|3.||Celli, Jacopo: 2 articles (05/2005 - 11/2003)|
|4.||Brunner, Han G: 2 articles (05/2005 - 11/2003)|
|5.||van Bokhoven, Hans: 2 articles (05/2005 - 11/2003)|
|6.||Han, Y-C: 1 article (09/2015)|
|7.||Patella, L: 1 article (09/2015)|
|8.||Fiori, E: 1 article (09/2015)|
|9.||Pascucci, T: 1 article (09/2015)|
|10.||Ventura, A: 1 article (09/2015)|
03/01/2014 - "Germline hemizygous deletions of MIR17HG are accounted for microcephaly, short stature, and digital abnormalities in a few cases of Feingold syndrome. "
05/01/2011 - "Feingold syndrome (FS) is a syndromic microcephaly entity for which MYCN is the major disease-causing gene. "
12/01/2010 - "In humans, mutation of N-myc also causes microcephaly in Feingold Syndrome. "
09/01/2007 - "Feingold syndrome is an important genetic cause of syndromic EA-TEF to consider in patients with associated microcephaly and digital anomalies. "
07/01/2005 - "We report a case of Feingold syndrome with oesophageal atresia and microcephaly. "
|2.||Learning Disorders (Learning Disability)
05/01/2005 - "Feingold syndrome is characterized by variable combinations of esophageal and duodenal atresias, microcephaly, learning disability, syndactyly and cardiac defect. "
09/01/2015 - "Feingold syndrome (FS) is an autosomal dominant disorder characterized by microcephaly, short stature, digital anomalies, esophageal/duodenal atresia, facial dysmorphism, and various learning disabilities. "
01/01/2009 - "Feingold syndrome (FS) is a dominantly inherited combination of microcephaly with or without learning disabilities, hand and foot abnormalities, short palpebral fissures and esophageal/duodenal atresia. "
02/01/2000 - "Oculodigitoesophageoduodenal (ODED) syndrome (also known as "Feingold syndrome") is a rare autosomal dominant disorder with digital abnormalities, microcephaly, short palpebral fissures, mild learning disability, and esophageal/duodenal atresia. "
11/28/1997 - "Feingold syndrome (or oculodigitoesophagoduodenal syndrome; Microcephaly, Mesobrachyphalangy, Tracheo-esophageal fistula syndrome) is a dominantly inherited combination of hand and foot abnormalities, microcephaly, esophageal/duodenal atresia, short palpebral fissures and learning disabilities, first reported in 1975 (MIM 164280). "
01/01/2012 - "[Association esophageal atresia type 3 - microcephaly: an incomplete Feingold syndrome?]."
12/01/2009 - "Feingold syndrome is a rare autosomal dominant condition that is characterized by variable expressivity of microcephaly, limb malformations, esophageal atresia, and a host of other malformations. "
09/01/2004 - "Feingold syndrome: microcephaly, esophageal atresia, type III laryngeal cleft, malrotation, limb anomalies."
07/01/2006 - "This is highlighted by the recent identification of no fewer than three separate genes with a role in the aetiology of oesophageal atresia: those for Feingold syndrome (N-MYC), anophthalmia-oesophageal-genital (AEG) syndrome (SOX2), and CHARGE syndrome (CHD7). "
01/01/2011 - "This differential diagnosis includes (but is not limited to) Baller-Gerold syndrome, CHARGE syndrome, Currarino syndrome, deletion 22q11.2 syndrome, Fanconi anemia, Feingold syndrome, Fryns syndrome, MURCS association, oculo-auriculo-vertebral syndrome, Opitz G/BBB syndrome, Pallister-Hall syndrome, Townes-Brocks syndrome, and VACTERL with hydrocephalus. "
|5.||Hearing Loss (Hearing Impairment)
10/01/1999 - "A case of Feingold syndrome is presented with a previously undescribed association of bilateral profound hearing impairment. "
11/01/2012 - "A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome."
11/01/2012 - "We report a 26-month-old girl with profound hearing impairment, microcephaly, psychomotor retardation, short palpebral fissures, hypertelorism, epicanthic folds, a broad nasal bridge, anteverted nostrils, large low-set ears, micrognathia, brachymesophalangy of the second and the fifth fingers, clinodactyly of bilateral fifth fingers and a wide interdigital space between the first and the second toes, carrying a 4.4-Mb de novo microdeletion of chromosome 2p24.3 → p24.2. This region contains the genes of FAM84A, NBAS, DDX1, MYCNOS and MYCN, of which haploinsufficiency or mutations of the MYCN gene is associated with Feingold syndrome. "
|1.||Familial duodenal atresia
|9.||Craniosynostosis radial aplasia syndrome