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  2. Chronic diarrhea of infancy - Wikipedia

    en.wikipedia.org/wiki/Chronic_diarrhea_of_infancy

    Toddler's diarrhea is characterized by three or more watery stools per day that persist for 2–4 weeks or more. [2] [6] Newborns and infants may normally have soft and frequent stools; however, any noticeable changes in stool frequency or form (i.e. watery) can indicate toddler's diarrhea. [7]

  3. Dwarfism - Wikipedia

    en.wikipedia.org/wiki/Dwarfism

    Dwarfism is a condition of people and animals marked by unusually small size or short stature. [1] In humans, it is sometimes defined as an adult height of less than 147 centimetres (4 ft 10 in), regardless of sex; the average adult height among people with dwarfism is 120 centimetres (4 ft).

  4. Cornelia de Lange syndrome - Wikipedia

    en.wikipedia.org/wiki/Cornelia_de_Lange_Syndrome

    Children with CdLS often have gastrointestinal tract difficulties, particularly gastroesophageal reflux. Vomiting, intermittent poor appetite, constipation, diarrhea or gaseous distention are known to be a regularity in cases where the GI tract problems are acute. Symptoms may range from mild to severe.

  5. Achondroplasia in children - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia_in_children

    Achondroplasia in children is the most common form of dwarfism; it accounts for about 70% of all cases of dwarfism. [1] Achondroplasia falls into the category of “disproportionate dwarfism”. It is linked to a mutation in the fibroblast growth factor receptor-3.

  6. Dwarfism, low-birth-weight type with unresponsiveness to ...

    en.wikipedia.org/wiki/Dwarfism,_low-birth-weight...

    Dwarfism, low-birth-weight type with unresponsiveness to growth hormone is a very rare genetic disorder which is characterized by developmental delays, intellectual disabilities, and other anomalies. Only 2 cases have been described in medical literature.

  7. Achondroplasia - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia

    Achondroplasia is a genetic disorder with an autosomal dominant pattern of inheritance whose primary feature is dwarfism. [3] It is the most common cause of dwarfism [4] and affects about 1 in 27,500 people. [3] In those with the condition, the arms and legs are short, while the torso is typically of normal length. [3]

  8. Silver–Russell syndrome - Wikipedia

    en.wikipedia.org/wiki/Silver–Russell_syndrome

    Silver–Russell syndrome, also called Silver–Russell dwarfism, is a rare congenital growth disorder. In the United States it is usually referred to as Russell–Silver syndrome, and Silver–Russell syndrome elsewhere. It is one of 200 types of dwarfism and one of five types of primordial dwarfism.

  9. Congenital chloride diarrhea - Wikipedia

    en.wikipedia.org/wiki/Congenital_chloride_diarrhea

    CCD may be detectable on prenatal ultrasound. [4] [5] After birth, signs in affected babies typically are abdominal distension, visible peristalsis, and watery stools persistent from birth that show chloride loss of more than 90 mmol/L. [5] An important feature in this diarrhea that helps in the diagnosis, is that it is the only type of diarrhea that causes metabolic alkalosis rather than ...