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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. Amish lethal microcephaly - Wikipedia

    en.wikipedia.org/wiki/Amish_lethal_microcephaly

    Amish lethal microcephaly is a rare genetic disorder which is characterized by severe microcephaly (small head) from birth, brain hypoplasia (underdeveloped brain), micrognathia (small chin), irritability (at second or third month of age), seizures, problems controlling their body temperature, high levels of alpha-ketogluraic acid in their urine, [2] and less commonly hepatomegaly (large liver).

  4. Achalasia microcephaly - Wikipedia

    en.wikipedia.org/wiki/Achalasia_microcephaly

    Achalasia microcephaly; Chest x-ray of an individual with achalasia. The arrows point to the areas of extreme esophageal dilation. Symptoms: Manifestation of achalasia: regurgitation, vomiting and dysphagia, alongside diagnosis of microcephaly: abnormally small head size below the third percentile as well as mild to moderate mental retardation.

  5. Seckel syndrome - Wikipedia

    en.wikipedia.org/wiki/Seckel_syndrome

    Seckel syndrome, or microcephalic primordial dwarfism (also known as bird-headed dwarfism, Harper's syndrome, Virchow–Seckel dwarfism and bird-headed dwarf of Seckel [1]) is an extremely rare congenital nanosomic disorder.

  6. Encephalocele - Wikipedia

    en.wikipedia.org/wiki/Encephalocele

    Encephaloceles are often accompanied by craniofacial abnormalities or other brain malformations. Symptoms may include neurologic problems, hydrocephalus (cerebrospinal fluid accumulated in the brain), spastic quadriplegia (paralysis of the limbs), microcephaly (an abnormally small head), ataxia (uncoordinated muscle movement), developmental delay, vision problems, mental and growth retardation ...

  7. Rubinstein–Taybi syndrome - Wikipedia

    en.wikipedia.org/wiki/Rubinstein–Taybi_syndrome

    Rubinstein–Taybi syndrome presents itself from birth, and is usually hallmarked by delayed physical and cognitive growth. [citation needed] Typical features of the disorder include: Broad thumbs and broad first toes and clinodactyly of the 5th finger [4] Mental disability; Small height, low bone growth, small head; Cryptorchidism in males

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    mail.aol.com

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  9. Cephalocaudal trend - Wikipedia

    en.wikipedia.org/wiki/Cephalocaudal_trend

    One example of this is the gradual change in head size relative to body size during human growth. During prenatal growth, from conception to 5 months, the head grows more than the body. In humans, the head comprises almost 50% of total body length at approximately the third month of intrauterine development. By the time of birth the head has ...