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2.
J Pediatr ; 93(3): 378-82, 1978 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-211214

RESUMEN

Two hundred children 7 to 14 years of age with isolated cleft defects of the lip, palate, or both were surveyed for stature. Twelve percent were less than the third percentile in height and were designated "short." All of the short children received an endocrine evaluation. Endogenous growth hormone was examined after two days' pretreatment with stilbesteral. Four of the 25 short children with CLP had total, and four had partial, GH deficiency. Three of the GH-deficient patients were also deficient in ACTH or TSH. In contrast, in a series of 75 short (less than third percentile) children 7 to 14 years of age without cleft defect or other apparent congenital abnormality, only two had total and two had partial GH deficiency. The data suggest that children with isolated CLP have short stature about four times more often, and GH-deficiency about 40 times more often, than children without CLP. The increased prevalence of GH-deficiency may stem from the embryologic relation of adenohypophysis and oral ectoderm.


Asunto(s)
Labio Leporino/complicaciones , Fisura del Paladar/complicaciones , Hormona del Crecimiento/deficiencia , Adolescente , Hormona Adrenocorticotrópica/deficiencia , Niño , Femenino , Trastornos del Crecimiento/etiología , Humanos , Masculino , Adenohipófisis/embriología , Tirotropina/deficiencia
3.
J Pediatr ; 87(5): 731-8, 1975 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-1185337

RESUMEN

A 9-year-old girl with hereditary dibasicaminoaciduria has been studied for three years. Initially, clinical features were: growth failure; anorexia and aversion to protein, spontaneous daily protein intake averaging only 10 gm; fasting and postprandial venous hyperammonemia; subnormal plasma concentrations of lysine, arginine, ornithine, and citrulline, with generalized hypermonobasicaminoacidemia; abnormally high renal clearances of lysine, arginine, and ornithine; and intestinal malabsorption of lysine and arginine. Intestinal absorption of citrulline, a precursor of arginine and ornithine, was normal. The patient was observed during four sequential 6-month periods as follows: no treatment (Period I); dietary supplement of arginine and lysine (Period II); dietary supplement of citrulline and lysine (Period III); no treatment (Period IV). During Periods II and III growth rate increased 3- to 4-fold, spontaneous protein intake increased 2- to 3-fold, and abnormalities in blood NH3 and the plasma aminogram were partially corrected. In most respects the citrulline plus lysine supplement was more beneficial than that of arginine plus lysine.


Asunto(s)
Errores Innatos del Metabolismo de los Aminoácidos/tratamiento farmacológico , Amoníaco/sangre , Arginina/uso terapéutico , Citrulina/uso terapéutico , Trastornos del Crecimiento/tratamiento farmacológico , Lisina/uso terapéutico , Niño , Femenino , Humanos
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