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  2. Polydactyly - Wikipedia

    en.wikipedia.org/wiki/Polydactyly

    Postaxial polydactyly. This is the most common situation, in which the extra digit is on the ulnar side of the hand, thus the side of the little finger. This can also be called postaxial polydactyly. It can manifest itself very subtly, for instance only as a nubbin on the ulnar side of the little finger, or very distinctly, as a fully developed ...

  3. Polysyndactyly - Wikipedia

    en.wikipedia.org/wiki/Polysyndactyly

    Preaxial polysyndactyly, in which the duplicated digit is on the side of the thumb or big toe, is less common. [3] Crossed polysyndactyly, in which polysyndactyly is present on the hand and foot, and is preaxial on one and postaxial on the other, is extremely rare and often occurs with other genetic disorders.

  4. Familial opposable triphalangeal thumbs duplication - Wikipedia

    en.wikipedia.org/wiki/Familial_opposable_tri...

    Familial opposable triphalangeal thumb duplication is a limb malformation syndrome and a type of pre-axial polydactyly, characterized by having duplicated opposable triphalangeal thumbs. This condition can be a symptom of other genetic disorders, such as Holt–Oram syndrome and Fanconi anemia .

  5. David Tennant announces that he was born with a rare condition

    www.aol.com/david-tennant-announces-born-rare...

    Polydactyly is a common congenital limb difference, occurring in about 1 in 500-1,000 live births. There are three types: pre-axial (extra digit near the thumb/big toe), post-axial (extra digit ...

  6. Scalp defects-postaxial polydactyly syndrome - Wikipedia

    en.wikipedia.org/wiki/Scalp_defects-postaxial...

    Scalp defects-postaxial polydactyly syndrome is a very rare genetic disorder which is characterized by congenital defects of the scalp and type A postaxial polydactyly. [1] [2] An additional finding is severe intellectual disability. It is thought to be inherited in an autosomal dominant manner.

  7. Bardet–Biedl syndrome - Wikipedia

    en.wikipedia.org/wiki/Bardet–Biedl_syndrome

    Bardet–Biedl syndrome is a pleiotropic disorder with variable expressivity and a wide range of clinical variability observed both within and between families. The most common clinical features are rod–cone dystrophy, with childhood-onset night-blindness followed by increasing visual loss; postaxial polydactyly; truncal obesity that manifests during infancy and remains problematic ...

  8. Ectrodactyly with tibia aplasia/hypoplasia - Wikipedia

    en.wikipedia.org/wiki/Ectrodactyly_with_tibia...

    Additional findings include cup-shaped ears, pre-postaxial polydactyly, and hypoplasia of the big toes, femur, patella, and ulnae bone. It is inherited as an autosomal dominant trait with reduced penetrance. [2] [3] [4]

  9. 30 things to do when you’re bored (that are actually good for ...

    www.aol.com/lifestyle/30-things-bored-actually...

    What’s your favorite screen-free thing to do when you’re bored? Share your tried-and-true anti-boredom tips in the comments below.