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  2. Buy One of These Snow Sleds for Plenty of Winter Family Fun - AOL

    www.aol.com/buy-one-snow-sleds-plenty-173800918.html

    Choose from heirloom-quality sleds, classic metal saucer sleds, and more. You and your family will be sleighing all day when you buy one or two of the best snow sleds! Choose from heirloom-quality ...

  3. Prepubertal hypertrichosis - Wikipedia

    en.wikipedia.org/wiki/Prepubertal_hypertrichosis

    Prepubertal hypertrichosis is characterized by an excess of hair growth, seen during birth and progressing during childhood. [3] [6] In generalized hypertrichosis, excessive hair growth occurs all over the body, whereas in localized hypertrichosis, excessive hair growth only occurs in certain areas of the body. [2]

  4. Noonan syndrome - Wikipedia

    en.wikipedia.org/wiki/Noonan_syndrome

    Noonan syndrome (NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. [1] Facial features include widely spaced eyes, light-colored eyes, low-set ears, a short neck, and a small lower jaw. [1]

  5. Child harness - Wikipedia

    en.wikipedia.org/wiki/Child_harness

    Child harnesses are most commonly used with toddlers and children of preschool age, though they may also be used with older children, especially if they have special supervisory needs such as ADHD or autism. Various types exist, though all are worn by the child and have a lead (tether) or rein which is held by a parent or caregiver.

  6. When does a pediatrician say it's OK to pierce a baby's ears?

    www.aol.com/lifestyle/cultural-tradition-child...

    But it's not just celebrities who come under scrutiny for choosing to pierce their baby's ears. When Monica Hammack of Houston, Tex. shared photos on Facebook of her then 9-month-old daughter's ...

  7. Saethre–Chotzen syndrome - Wikipedia

    en.wikipedia.org/wiki/Saethre–Chotzen_syndrome

    The mouse TWIST gene is located on chromosome 12 in mice, which corresponds to the short arm of chromosome 7 in humans. With this information, scientists began to isolate and map the human TWIST gene on the short arm of human chromosome 7. They revealed that the human TWIST gene was in the same region that was absent in people with SCS.