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Feingold syndrome (medical condition): A very rare syndrome characterized mainly by a small head and gastrointestinal...more »
See also:
Oculodigitoesophagoduodenal syndrome:
»Introduction: Oculodigitoesophagoduodenal syndrome
»Symptoms of Oculodigitoesophagoduodenal syndrome
Feingold syndrome: Microcephaly, type A brachydactyly, short stature, duodenal atresia, patent ductus arteriosus, hallux valgus, restricted finger and elbow movement, and syndactyly of the toes. Learning disability occurs in about one-third of the affected infants. Dysplasia of diaphyseal ossification centers is the cause of digital anomalies.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Feingold syndrome:
Feingold syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Feingold syndrome, or a subtype of Feingold syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Feingold syndrome as a "rare disease".
Source - Orphanet
Feingold syndrome: Another name for Oculodigitoesophagoduodenal syndrome (or close medical condition association).
»Introduction: Oculodigitoesophagoduodenal syndrome
»Symptoms of Oculodigitoesophagoduodenal syndrome
Feingold syndrome: Feingold syndrome is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Feingold syndrome incude:
See full list of 21 symptoms of Feingold syndrome (Oculodigitoesophagoduodenal syndrome)
Source: Diseases Database
Source - NIH
Source: Diseases Database
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