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Disease Profile
Congenital tracheal stenosis
Prevalence estimates on Rare Medical Network websites are calculated based on data available from numerous sources, including US and European government statistics, the NIH, Orphanet, and published epidemiologic studies. Rare disease population data is recognized to be highly variable, and based on a wide variety of source data and methodologies, so the prevalence data on this site should be assumed to be estimated and cannot be considered to be absolutely correct.
0
Age of onset
Neonatal
ICD-10
Q32.1
Inheritance
Autosomal dominant A pathogenic variant in only one gene copy in each cell is sufficient to cause an autosomal dominant disease.
Autosomal recessive Pathogenic variants in both copies of each gene of the chromosome are needed to cause an autosomal recessive disease and observe the mutant phenotype.
X-linked
dominant X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
dominant X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome.
X-linked
recessive Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder.
recessive Pathogenic variants in both copies of a gene on the X chromosome cause an X-linked recessive disorder.
Mitochondrial or multigenic Mitochondrial genetic disorders can be caused by changes (mutations) in either the mitochondrial DNA or nuclear DNA that lead to dysfunction of the mitochondria and inadequate production of energy.
Multigenic or multifactor Inheritance involving many factors, of which at least one is genetic but none is of overwhelming importance, as in the causation of a disease by multiple genetic and environmental factors.
Not applicable
Other names (AKA)
Tracheobronchial stenosis, congenital
Categories
Congenital and Genetic Diseases; Ear, Nose, and Throat Diseases
Symptoms
This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.
Medical Terms | Other Names |
Learn More:
HPO ID
|
---|---|---|
80%-99% of people have these symptoms | ||
Weak cry | 0001612 | |
30%-79% of people have these symptoms | ||
5-minute APGAR score of 3 | 0030923 | |
Anomalous origin of left pulmonary artery from ascending aorta | 0011661 | |
Polyhydramnios |
High levels of amniotic fluid
|
0001561 |
Respiratory distress |
Breathing difficulties
Difficulty breathing
[ more ] |
0002098 |
Wheezing | 0030828 | |
5%-29% of people have these symptoms | ||
Abnormal lung lobation | 0002101 | |
Abnormal stomach morphology | 0002577 | |
Abnormality of earlobe |
Abnormal earlobe
Abnormality of ear lobe
[ more ] |
0000363 |
Abnormality of the kidney |
Abnormal kidney
|
0000077 |
Abnormality of the ureter | 0000069 | |
Anal atresia |
Absent anus
|
0002023 |
Ascending aorta hypoplasia | 0031935 | |
Cyanosis |
Blue discoloration of the skin
|
0000961 |
Duodenal atresia |
Absence or narrowing of first part of small bowel
|
0002247 |
Duodenal stenosis | 0100867 | |
Fetal ascites | 0001791 | |
Meckel diverticulum | 0002245 | |
Neonatal asphyxia | 0012768 | |
Oligohydramnios |
Low levels of amniotic fluid
|
0001562 |
Patent ductus arteriosus | 0001643 | |
Preductal coarctation of the aorta | 0005151 | |
Pulmonary artery atresia | 0004935 | |
Tracheoesophageal fistula | 0002575 | |
Ventricular septal defect |
Hole in heart wall separating two lower heart chambers
|
0001629 |
1%-4% of people have these symptoms | ||
Abnormal bronchus morphology | 0025426 | |
Abnormality of the nervous system |
Neurologic abnormalities
Neurological abnormality
[ more ] |
0000707 |
Hypoplastic left heart |
Underdeveloped left heart
|
0004383 |
Upper airway obstruction | 0002781 |
Organizations
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
Organizations Supporting this Disease
-
Tracheo-Oesophageal Fistula Support (TOFS)
St. George’s Centre
91 Victoria Road
Netherfield
Nottingham, NG4 2NN United Kingdom
Telephone: +44 (0)115 961 3092
E-mail: [email protected]
Website: https://www.tofs.org.uk/home.aspx
Learn more
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
In-Depth Information
- The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
- Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.