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The etiology of VACTERL association: Current knowledge and hypotheses
- Source :
- American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 178:440-446
- Publication Year :
- 2018
- Publisher :
- Wiley, 2018.
-
Abstract
- VACTERL association is a condition involving the presence of multiple congenital anomalies. The condition was first described more than four decades ago, and is not extremely rare. However, relatively little is understood about the causes and underlying biology of the condition as a whole. There are many reasons for this, but there is increasing recognition that VACTERL is extremely clinically as well as etiologically heterogeneous, and this heterogeneity--as well as other hypothesized factors--have caused challenges to identifying the causes for a substantial proportion of patients. Current knowledge about the causes of this condition (or group of conditions) are described, followed by a discussion of possibilities that may reveal more answers for patients as well as researchers and clinicians who work related to this disorder.
- Subjects :
- Heart Defects, Congenital
0301 basic medicine
Pediatrics
medicine.medical_specialty
Limb Deformities, Congenital
Anal Canal
030105 genetics & heredity
Kidney
medicine.disease
VACTERL association
Work related
Spine
Trachea
03 medical and health sciences
Esophagus
Genetics
medicine
Etiology
Humans
Abnormalities, Multiple
Genetics (clinical)
Subjects
Details
- ISSN :
- 15524868
- Volume :
- 178
- Database :
- OpenAIRE
- Journal :
- American Journal of Medical Genetics Part C: Seminars in Medical Genetics
- Accession number :
- edsair.doi.dedup.....fea85ec1ab38e24d502cc76e13bc5d7c
- Full Text :
- https://doi.org/10.1002/ajmg.c.31664