Feingold syndrome | About the Disease | GARD - Genetic and …
A rare genetic, congenital malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies (brachymesophanlangy, fifth finger clinodactyly, syndactyly of …
Feingold syndrome - Wikipedia
Feingold syndrome (also called oculodigitoesophagoduodenal syndrome) is a rare autosomal dominant hereditary disorder. It is named after Murray Feingold, an American physician who …
Feingold Syndrome 1 - GeneReviews® - NCBI Bookshelf
2009年6月30日 · Feingold syndrome 1 (FS1) as described by Feingold [1975] and Brunner & Winter [1991] is characterized by digital anomalies, microcephaly, facial dysmorphism, …
Feingold syndrome - MedlinePlus
Feingold syndrome is a disorder that affects many parts of the body. There are two types of Feingold syndrome, distinguished by their genetic cause; both types have similar features that …
Feingold syndrome - National Organization for Rare Disorders
Feingold syndrome (FS), also known as oculo-digito-esophageal-duodenal (ODED) syndrome, is a rare inherited malformation syndrome characterized by microcephaly, short stature and …
Feingold syndrome - Orphanet
A rare genetic, congenital malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies (brachymesophanlangy, fifth finger clinodactyly, syndactyly of …
Feingold syndrome - NIH Genetic Testing Registry (GTR) - NCBI
There are two types of Feingold syndrome, distinguished by their genetic cause; both types have similar features that can vary among affected individuals.\n\nIndividuals with Feingold …
Orphanet: Feingold syndrome type 1
A rare, genetic congenital malformation syndrome characterized by digital anomalies (shortening of the 2nd and 5th middle phalanx of the hand, clinodactyly of the 5th finger, syndactyly of toes …
Feingold syndrome (Concept Id: C0796068) - National Center for ...
Feingold syndrome is a disorder that affects many parts of the body. There are two types of Feingold syndrome, distinguished by their genetic cause; both types have similar features that …
FDNA™ Feingold syndrome: Key Symptoms, Causes, and Diagnosis
Feingold syndrome is a rare genetic syndrome that affects multiple parts of the body. There are two types of the condition: Type 1 and Type 2, each with their own genetic cause.