Type IV Laryngotracheoesophageal Cleft Associated with Type III Esophageal Atresia in 1p36 Deletions Containing the RERE Gene: Is There a Causal Role for the Genetic Alteration?
The causes of embryological developmental anomalies leading to laryngotracheoesophageal clefts (LTECs) are not known, but are proposed to be multifactorial, including genetic and environmental factors. Haploinsufficiency of the RERE gene might contribute to different phenotypes seen in individuals w...
Saved in:
| Main Authors: | Gloria Pelizzo, Aurora Puglisi, Maria Lapi, Maria Piccione, Federico Matina, Martina Busè, Giovanni Battista Mura, Giuseppe Re, Valeria Calcaterra |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Wiley
2018-01-01
|
| Series: | Case Reports in Pediatrics |
| Online Access: | http://dx.doi.org/10.1155/2018/4060527 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Gastric tumor mimicking bronchial tissue associated with a laryngotracheoesophageal cleft: a case report
by: Erika Nakatani, et al.
Published: (2023-05-01) -
P321: Identifying new genotype/phenotype correlations for individuals carrying deleterious RERE variants
by: David Curtis, et al.
Published: (2025-01-01) -
Intermediate type pulmonary atresia with intact ventricular septum
by: R Doğan, et al.
Published: (1995-04-01) -
Diagnostic value of prenatal ultrasound in the typing of fetal esophageal atresia
by: Lijun Song, et al.
Published: (2025-07-01) -
Ileal atresia and total colonic hirschsprung disease in a 36‐week neonate: A case report
by: Khashahyar Atqiaee, et al.
Published: (2023-03-01)