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  2. Arachnodactyly - Wikipedia

    en.wikipedia.org/wiki/Arachnodactyly

    Causes Mutations in the fibrillin-2 gene, in chromosome 5q23, or the fibrillin-1 gene, at chromosome 15q21.1 Arachnodactyly (" spider fingers ") is a medical condition that is characterized by fingers and toes that are abnormally long and slender, in comparison to the palm of the hand and arch of the foot.

  3. Pigeon toe - Wikipedia

    en.wikipedia.org/wiki/Pigeon_toe

    Pigeon toe, also known as in-toeing, is a condition which causes the toes to point inward when walking.It is most common in infants and children under two years of age [1] and, when not the result of simple muscle weakness, [2] normally arises from underlying conditions, such as a twisted shin bone or an excessive anteversion (femoral head is more than 15° from the angle of torsion) resulting ...

  4. Clubfoot - Wikipedia

    en.wikipedia.org/wiki/Clubfoot

    At first, the brace is worn full-time (23 hours per day) on both feet, regardless of whether the clubfoot affects one or two feet. After 3 months of 23/7 wear, the brace is worn less frequently by gradually reducing hours a couple at a time, every couple months so that hours are down to 12–14 per day at or around a year old.

  5. Rubinstein–Taybi syndrome - Wikipedia

    en.wikipedia.org/wiki/Rubinstein–Taybi_syndrome

    Causes mutation or deletion in the CREBBP gene, located on chromosome 16, and/or the EP300 gene, located on chromosome 22. Rubinstein–Taybi syndrome ( RTS ) is a rare genetic condition characterized by short stature, moderate to severe learning difficulties, distinctive facial features, and broad thumbs and first toes. [ 2 ]

  6. These Pictures Will Help You Identify the Most Common ... - AOL

    www.aol.com/pictures-help-identify-most-common...

    What it looks like: Psoriasis causes patches of thickened skin, most often with silver, scaly flakes. It’s usually found around the elbows, feet, knees, palms, and you can even have scalp psoriasis.

  7. 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]

  8. Pediatric podiatry - Wikipedia

    en.wikipedia.org/wiki/Pediatric_podiatry

    Pes cavus or high arched feet are an unusual finding in young children. Whilst some cavus foot types are familial and normally inherited, others are indicative of genetic neurological conditions, e.g. Charcot–Marie–Tooth disease [10] or Friedrich's ataxia. The appearance of high arched feet in young children should be noted. [clarification ...

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