Congenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes
of unexplained fever, anhidrosis (inability to sweat), absence of reaction to noxious stimuli, …

Hereditary juvenile megaloblastic anemia due to vitamin B 12 (cobalamin) deficiency is
caused by intestinal malabsorption of cobalamin. In Imerslund–Gräsbeck syndrome (IGS), …

Background Neonatal suppurative parotitis is a rare disease. Only 32 cases were reported
in the English‐language literature between 1970 and 2004. Methods We searched Medline …

Selective intestinal malabsorption of vitamin B 12 causing juvenile megaloblastic anemia (MGA;
MIM# 261100) is a recessively inherited disorder that is believed to be rare except for …

Congenital insensitivity to pain with anhidrosis is an autosomal recessive hereditary
disorder characterized by recurrent episodic fever, anhidrosis (inability to sweat), absence of …

Phosphate enema is described as a safe and ideal method in preparing a child's bowel for
colonoscopy (1). However, phosphate toxicity associated with enterally administered sodium …

sensory and autonomic neuropathy type 4) is a rare autosomal reces-sive disease, and
about 33 cases have been previously reported. Complete morphologic and morphometric …

Sexual dimorphic studies of various parameters of the femur play an important role in forensic
studies. Various femur morphometric parameters help estimate an individual’s age, sex, …

The experimental trial was carried out to evaluate the impact of a mixture of Bacillus subtilis
and Bacillus licheniformis probiotic supplementation via the drinking water (AVI-GROW®) …

We studied Guillain-Barré syndrome, affecting children 12 years old or less, throughout Kuwait,
in the period between January 1, 1992, and March 31, 1997. Nineteen children had the …