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  2. Microcephaly - Wikipedia

    en.wikipedia.org/wiki/Microcephaly

    Microcephaly (from Neo-Latin microcephalia, from Ancient Greek μικρός mikrós "small" and κεφαλή kephalé "head" [2]) is a medical condition involving a smaller-than-normal head. [3] Microcephaly may be present at birth or it may develop in the first few years of life. [3]

  3. Hypospadias - Wikipedia

    en.wikipedia.org/wiki/Hypospadias

    Hypospadias is a common malformation in fetal development of the penis in which the urethra does not open from its usual location on the head of the penis. It is the second-most common birth defect of the male reproductive system, affecting about one of every 250 males at birth, [3] although when including milder cases, is found in up to 4% of newborn males. [4]

  4. Seckel syndrome - Wikipedia

    en.wikipedia.org/wiki/Seckel_syndrome

    It is believed to be caused by defects of genes on chromosome 3 and 18. One form of Seckel syndrome can be caused by mutation in the gene encoding the ataxia telangiectasia and Rad3-related protein which maps to chromosome 3q22.1–q24. This gene is central in the cell's DNA damage response and repair mechanism. Types include: [6]

  5. Birth defect - Wikipedia

    en.wikipedia.org/wiki/Birth_defect

    Birth defect is a widely used term ... Microcephaly is a disorder in which the fetus has an atypically small head, ... Prevalence of men was recorded for the ...

  6. Fetal hydantoin syndrome - Wikipedia

    en.wikipedia.org/wiki/Fetal_hydantoin_syndrome

    About one third of children whose mothers are taking this drug during pregnancy typically have intrauterine growth restriction with a small head and develop minor dysmorphic craniofacial features (microcephaly and intellectual disability) and limb defects including hypoplastic nails and distal phalanges (birth defects).

  7. Baby with extremely rare defect born with one eye in middle ...

    www.aol.com/news/2015-10-06-baby-with-extremely...

    Dr. Ahmed Badruddin, the baby's doctor, says that the boy has a full head of hair and very large ears. In addition to only having one eye, the baby has a number of other deformities on his body.

  8. Aarskog–Scott syndrome - Wikipedia

    en.wikipedia.org/wiki/Aarskog–Scott_syndrome

    X-linked recessive inheritance. Mutations in the FGD1 gene are the only known genetic cause of Aarskog-Scott syndrome. The FGD1 gene provides instructions for making a protein that turns on (activates) another protein called Cdc42, which transmits signals that are important for various aspects of development before and after birth.

  9. Why some people have a small hole in front of their upper ears

    www.aol.com/lifestyle/2016-11-29-why-some-people...

    There is a birth defect of the ear that is visible and relatively common around the world. It is called preauricular sinus which, according to the U.S. National Institutes of Health, or NIH ...