[Hypophosphatasia with normal urinary phosphoethanolamine in a 22-month-old girl].
1980
S Tecza, and
J Prandota, and
Z Morawska, and
M Rudzka, and
L Panków-Prandota
UI
MeSH Term
Description
Entries
D007014
Hypophosphatasia
A genetic metabolic disorder resulting from serum and bone alkaline phosphatase deficiency leading to hypercalcemia, ethanolamine phosphatemia, and ethanolamine phosphaturia. Clinical manifestations include severe skeletal defects resembling vitamin D-resistant rickets, failure of the calvarium to calcify, dyspnea, cyanosis, vomiting, constipation, renal calcinosis, failure to thrive, disorders of movement, beading of the costochondral junction, and rachitic bone changes. (From Dorland, 27th ed)
Hypophosphatasias
D007223
Infant
A child between 1 and 23 months of age.
Infants
D009943
Organophosphorus Compounds
Organic compounds that contain phosphorus as an integral part of the molecule. Included under this heading is broad array of synthetic compounds that are used as PESTICIDES and DRUGS.