When.com Web Search

  1. Including results for

    short root anomaly

    Search only for short root anomoly

Search results

  1. Results From The WOW.Com Content Network
  2. Ankyloglossia - Wikipedia

    en.wikipedia.org/wiki/Ankyloglossia

    Ankyloglossia, also known as tongue-tie, is a congenital oral anomaly that may decrease the mobility of the tongue tip [1] and is caused by an unusually short, thick lingual frenulum, a membrane connecting the underside of the tongue to the floor of the mouth. [2]

  3. Chromosome abnormality - Wikipedia

    en.wikipedia.org/wiki/Chromosome_abnormality

    A chromosomal abnormality, chromosomal anomaly, chromosomal aberration, chromosomal mutation, or chromosomal disorder is a missing, extra, or irregular portion of chromosomal DNA. [ 1 ] [ 2 ] These can occur in the form of numerical abnormalities, where there is an atypical number of chromosomes, or as structural abnormalities, where one or ...

  4. Anomaly matching condition - Wikipedia

    en.wikipedia.org/wiki/Anomaly_matching_condition

    Another way to prove the anomaly matching for continuous symmetries is to use the anomaly inflow mechanism. [4] To be specific, we consider four-dimensional spacetime in the following. For global continuous symmetries G {\displaystyle G} , we introduce the background gauge field A {\displaystyle A} and compute the effective action Γ [ A ...

  5. Eccentric anomaly - Wikipedia

    en.wikipedia.org/wiki/Eccentric_anomaly

    In orbital mechanics, the eccentric anomaly is an angular parameter that defines the position of a body that is moving along an elliptic Kepler orbit. The eccentric anomaly is one of three angular parameters ("anomalies") that define a position along an orbit, the other two being the true anomaly and the mean anomaly .

  6. SHORT syndrome - Wikipedia

    en.wikipedia.org/wiki/SHORT_syndrome

    SHORT syndrome is an uncommon autosomal-dominant condition marked by ocular depression, Rieger anomaly, teething delay, small height, hyperextensibility of joints, and/or hernias. It was characterized in 1975.

  7. 6-Year-Old Boy Who Was Born Blind Gets Vision Partially ...

    www.aol.com/6-old-boy-born-blind-195954930.html

    A Connecticut boy is among four children all born with severe childhood blindness who gained “life-changing improvements” to their vision after an experimental trial of gene therapy. Jace was ...

  8. Clinodactyly - Wikipedia

    en.wikipedia.org/wiki/Clinodactyly

    Clinodactyly is an autosomal dominant trait that has variable expressiveness and incomplete penetrance. [citation needed]Clinodactyly can be passed through inheritance and presents as either an isolated anomaly or a component manifestation of a genetic syndrome. [2]

  9. Hypodontia - Wikipedia

    en.wikipedia.org/wiki/Hypodontia

    Hypodontia is defined as the developmental absence of one or more teeth excluding the third molars.It is one of the most common dental anomalies, and can have a negative impact on function, and also appearance.