Find all needed information about Oculodentodigital Dysplasia Support. Below you can see links where you can find everything you want to know about Oculodentodigital Dysplasia Support.
https://rarediseases.info.nih.gov/diseases/7239/1
Oculodentodigital dysplasia is a condition that affects many parts of the body, including the eyes (oculo-), teeth (dento-), and fingers (digital). Symptoms of the condition include having small eyes, vision loss, missing teeth, frequent cavities, and bony growths in the fingers.
https://ghr.nlm.nih.gov/condition/oculodentodigital-dysplasia
Oct 01, 2019 · Oculodentodigital dysplasia is a condition that affects many parts of the body, particularly the eyes (oculo-), teeth (dento-), and fingers (digital). Common features in people with this condition are small eyes (microphthalmia) and other eye abnormalities that can lead to vision loss.Affected individuals also frequently have tooth abnormalities, such as small or missing teeth, …
https://rarediseases.org/rare-diseases/oculo-dento-digital-dysplasia/
Oculo-dento-digital dysplasia is a rare disorder characterized by webbing of the fourth and fifth fingers, an abnormally small transparent front part of the eye (cornea), a slender nose, underdeveloped outer walls of each nostril, narrowing of the nostrils, defective …
https://globalgenes.org/disease/oculodentodigital-dysplasia/
Oculodentodigital dysplasia (ODDD) is a rare genetic disorder affecting the eyes (oculo-), teeth (dento-), and fingers or toes (digital). Individuals with ODDD may be born with small eyes or other eye abnormalities that cause vision loss, small teeth that have a weak outer layer (enamel), and extra skin (webbing) between the fingers or toes (syndactyly).
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4869463/
Oculodentodigital dysplasia is a rare, autosomal dominant disorder with high penetrance and variable expressivity, caused by mutations in the connexin 43 or gap junction protein alpha-1 gene. It has been diagnosed in fewer than 300 people worldwide with an incidence of around 1 in 10 million.
https://www.dovemed.com/diseases-conditions/oculo-dento-digital-dysplasia/
Dec 11, 2018 · Oculo-Dento-Digital Dysplasia (ODDD) is a condition that affects the eyes, teeth, and fingers. Individuals affected by this condition commonly have abnormalities of the eye (small eyes, vision loss), teeth (small teeth, weak enamel, early tooth loss), and skin web between fingers.
https://www.sciencedirect.com/topics/medicine-and-dentistry/oculodentodigital-dysplasia
Oculodentodigital Dysplasia. Oculodentodigital dysplasia (ODDD) is a rare autosomal dominant disorder characterized by craniofacial anomalies involving the teeth and skull, as well as fusion of the digits, as the name would suggest.
https://www.diseaseinfosearch.org/disease/5319
Oculodentodigital dysplasia (ODDD) is a rare genetic disorder affecting the eyes (oculo-), teeth (dento-), and fingers or toes (digital). Individuals with ODDD may be born with small eyes or other eye abnormalities that cause vision loss, small teeth that have a weak outer layer (enamel), and extra skin (webbing) between the fingers or toes (syndactyly).
https://en.wikipedia.org/wiki/Oculodentodigital_dysplasia
Oculodentodigital syndrome (ODD syndrome) is an extremely rare genetic condition that typically results in small eyes, underdeveloped teeth, and syndactyly and malformation of the fourth and fifth fingers. It is considered a kind of ectodermal dysplasiaOther names: Oculo-dento-digital syndrome, Oculodentodigital dysplasia , and Oculodentoosseous dysplasia
https://www.nfed.org/learn/types/oculodentodigital-syndrome/
A physician can diagnose oculodentodigital syndrome on the basis of physical features. Causes of ODDD Syndrome ODDD is a condition caused by a change in the connexin 43 gene GJA1.
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