Alports’s Syndrome and Benign Familial Haematuria
Authors:
J. Janda; J. Dušek; K. Vondrák; J. Stejskal; Š. Krejčová
Authors‘ workplace:
I. dětská klinika 2. LF UK, FNsP v Motole, Praha, přednosta doc. MUDr. J. Janda, CSc. Ústav patologické anatomie 2. LF UK, FNsP v Motole, Praha, přednosta prof. MUDr. R. Kodet, CSc. Ústav biologie a klinické genetiky 2. LF UK, FNsP v Motole, Praha, předno
Published in:
Čes-slov Pediat 1999; (10): 602-609.
Category:
Overview
Alport’s syndrome (AS) and benign familial haematuria (BFH) are congenital nephropathies with a differentprognosis. The authors present, based on a review of contemporary literature, detailed diagnostic possibilities ofboth clinical entities. They draw attention in particular to the high rate of BFH in children with intractablehaematuria. The authors mention recent advances in molecular diagnosis of AS and BFH incl. activities in theCzech Republic. Paediatricians should be well informed on this problem as child patients can in many instancesbe spared (in particular in BFH) unnecessary invasive examinations.
Key words:
Alport’s syndrome, benign familial haematuria, clinical, morphological and molecular geneticdiagnosis
Labels
Neonatology Paediatrics General practitioner for children and adolescentsArticle was published in
Czech-Slovak Pediatrics
1999 Issue 10
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