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  2. Polydactyly - Wikipedia

    en.wikipedia.org/wiki/Polydactyly

    It is most frequent in Indian populations and it is the second most common congenital hand disorder. ... six fingers on each hand (the ... with a dominant gene at one ...

  3. Polysyndactyly - Wikipedia

    en.wikipedia.org/wiki/Polysyndactyly

    Polysyndactyly is typically inherited, in an autosomal dominant pattern. [2] [6] [9] The specific mutations leading to polysyndactyly are varied between among types of the condition and different families. However, many cases are caused by changes to genetic elements affecting the signaling molecule Sonic Hedgehog (SHH).

  4. Greig cephalopolysyndactyly syndrome - Wikipedia

    en.wikipedia.org/wiki/Greig_cephalopolysyndactyl...

    This condition is inherited in an autosomal dominant pattern, which means the defective gene is located on an autosome, and only one copy of the defective GLI3 gene is sufficient to cause the disorder. In cases of dominant inheritance, an affected person inherits the genetic mutation or chromosomal abnormality from one affected parent. [1]

  5. Brachydactyly - Wikipedia

    en.wikipedia.org/wiki/Brachydactyly

    Nomograms for normal values of finger length as a ratio to other body measurements have been published. In clinical genetics, the most commonly used index of digit length is the dimensionless ratio of the length of the third (middle) finger to the hand length. Both are expressed in the same units (centimeters, for example) and are measured in ...

  6. Brachydactyly type D - Wikipedia

    en.wikipedia.org/wiki/Brachydactyly_type_D

    A genetic trait, brachydactyly type D exhibits autosomal dominance and is commonly developed or inherited independently of other hereditary traits. The condition is associated with the HOXD13 gene, which is central in digital formation and growth. [5] Various other studies supported an autosomal dominant pattern with reduced penetrance. [8]

  7. Severe achondroplasia with developmental delay and acanthosis ...

    en.wikipedia.org/wiki/Severe_Achondroplasia_with...

    Autosomal means that the gene responsible for the mutation and disorder is found on a non-sex chromosome and that either the mother or father can pass on the gene, while dominant means that only one copy of the gene is required for the individual to have the disorder. The disorder is very rare and has only been described in a few number of ...

  8. Syndactyly - Wikipedia

    en.wikipedia.org/wiki/Syndactyly

    In early human fetal development, webbing (syndactyly) of the toes and fingers is normal. At about 6 weeks of gestation, apoptosis takes place due to a protein named sonic hedgehog, also known as SHH, which dissolves the tissue between the fingers and toes, and the webbing disappears. In some fetuses, this process does not occur completely ...

  9. Camptodactyly - Wikipedia

    en.wikipedia.org/wiki/Camptodactyly

    Camptodactyly is a medical condition that causes one or more digits (fingers or toes) to be permanently bent. It involves fixed flexion deformity of the proximal interphalangeal joints. Camptodactyly can be caused by a genetic disorder. In that case, it is an autosomal dominant trait that is known for its incomplete genetic expressivity. This ...