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[Efficacy of dietetic treatment in a case of galactosemia diagnosed late].
Pediatr Med Chir. 1982 Nov-Dec; 4(6):685-6.PM

Abstract

The authors describe a six months old girl affected by galactosemia, due to Galacto-1-phosphate Uridyl Transferase deficiency. The patient presented with hepatosplenomegaly and failure to thrive, without neurological impairment or cataracts. In this case removal of galactose from diet, although lately performed, resulted in normal growth and development. The authors emphasize the importance of ruling out galactosemia, even if clinical picture is unusual.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
English Abstract
Journal Article

Language

ita

PubMed ID

6927423

Citation

Sebastio, G, et al. "[Efficacy of Dietetic Treatment in a Case of Galactosemia Diagnosed Late]." La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics, vol. 4, no. 6, 1982, pp. 685-6.
Sebastio G, Albini F, di Martino L, et al. [Efficacy of dietetic treatment in a case of galactosemia diagnosed late]. Pediatr Med Chir. 1982;4(6):685-6.
Sebastio, G., Albini, F., di Martino, L., Magurno, T., Baffa, E., & Ciaffoni, F. (1982). [Efficacy of dietetic treatment in a case of galactosemia diagnosed late]. La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics, 4(6), 685-6.
Sebastio G, et al. [Efficacy of Dietetic Treatment in a Case of Galactosemia Diagnosed Late]. Pediatr Med Chir. 1982 Nov-Dec;4(6):685-6. PubMed PMID: 6927423.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - [Efficacy of dietetic treatment in a case of galactosemia diagnosed late]. AU - Sebastio,G, AU - Albini,F, AU - di Martino,L, AU - Magurno,T, AU - Baffa,E, AU - Ciaffoni,F, PY - 1982/11/1/pubmed PY - 1982/11/1/medline PY - 1982/11/1/entrez SP - 685 EP - 6 JF - La Pediatria medica e chirurgica : Medical and surgical pediatrics JO - Pediatr Med Chir VL - 4 IS - 6 N2 - The authors describe a six months old girl affected by galactosemia, due to Galacto-1-phosphate Uridyl Transferase deficiency. The patient presented with hepatosplenomegaly and failure to thrive, without neurological impairment or cataracts. In this case removal of galactose from diet, although lately performed, resulted in normal growth and development. The authors emphasize the importance of ruling out galactosemia, even if clinical picture is unusual. SN - 0391-5387 UR - https://www.unboundmedicine.com/medline/citation/6927423/[Efficacy_of_dietetic_treatment_in_a_case_of_galactosemia_diagnosed_late]_ L2 - http://www.diseaseinfosearch.org/result/2973 DB - PRIME DP - Unbound Medicine ER -