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Z Szelid

Publications and source records attributed to Z Szelid.

10 recordsLinked to original sources

Long-term follow-up of patients with persistent/recurrent, isolated haematuria: a Hungarian multicentre study.

A retrospective multicentre study of 341 children with persistent/recurrent, isolated haematuria is described. The haematuria was isolated for at least 6 months at the beginning of observation. The duration of follow-up was 2-5 years in 201, 5-10 years in 119, 10-15 years in 19, and over 15 years in 2 cases. Of these patients 47.8% became symptom-free. In 18.4% the haematuria remained isolated; in 13.8% it was combined with proteinuria over 250 mg/day more than 2 years later. The occurrence of associated proteinuria increased progressively with time. It was 8.6% between the 3rd and 5th years, and 37.0% after the 5th year. Renal biopsy was performed because of the symptoms of glomerular disease in 47 cases at an average time of 12 months following the appearance of proteinuria. Proteinuria appeared after a 2-5, 5-10, 10-15 and more than 15 years follow-up period in 16, 23, 6, and 2 patients respectively; 14 of them had Alport's nephropathy. The percentage of more serious azotaemia was 1.7 (creatinine clearance: 10-50 ml/min per 1.73 m2) and 0.3 (creatinine clearance: less than 10 ml/min per 1.73 m2). Mortality was 0.58%. Most of the patients who developed severe azotaemia had persistent microscopic haematuria at the beginning. The prevalence of hypertension was only 1.2%. The time of its appearance was above 5 years in 2 and below 5 years in 2 cases. All these patients had chronic glomerulonephritis. The haematuria was associated with hypercalciuria in 19.9%. In 14.3% of the overall group of patients urolithiasis developed 2-15 years after onset. All of these had hypercalciuria.(ABSTRACT TRUNCATED AT 250 WORDS)

Child↗

Autosomal dominant inheritance of hypercalciuria.

We examined 37 first and second degree relatives of 10 children with hypercalciuria. In 2 families only the index patient was affected, while in 8 others one of the parents was hypercalciuric; in the total of 47 persons examined 23 cases of "idiopathic" hypercalciuria could be identified. None of the subjects was hypercalcemic. The pedigrees suggest autosomal dominant inheritance of the trait.

Adolescent↗

[Liver function in acute urinary tract infection].

Association of pyelonephritis with icterus has been observed in 26 young infants. The observations suggest that in the case of early infantile hyperbilirubinaemia it is important to search for urinary tract infection which may remain an asymptomatic bacteriuria. Liver function tests were performed in 21 children aged 1 month to 8 years suffering from pyelonephritis without hyperbilirubinaemia. In 6 infants a pathologic BSP-retention was found, probably due to toxic effects of Gram-negative bacteria. It is concluded that BSP-retention might indicate the severity of the disease.

Acute Disease↗

Physical growth of children born small for gestational age.

In a longitudinal study the postnatal physical growth of 188 small for gestational age and 225 appropriate for gestational age children was compared. A significant retardation in weight, stature, head circumference and osseous development of SGA children was observed even at the age of 3 years.

Anthropometry↗

Possible dominant inheritance of the idiopathic hypercalcemic syndrome.

A girl, aged 16 months, with idiopathic hypercalcemia (failure to thrive, characteristic face, supravalvular aortic stenosis) was observed. Her serum calcium level was between 14 and 20 mg/100 ml. Both her father and brother were mentally retarded and had calcium deposits in their corneae. Their serum calcium values were 11.9 and 13.0 mg/100 ml, respectively, with increased urinary output of calcium. The family history is suggestive of autosomal dominant inheritance of the disease.

Adolescent↗