GENETIC DISORDERS - DEVELOPMENT: Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen A alpha chain gene

Background. Systemic amyloidosis occurring in early childhood is extremely rare, and is usually of AA type complicating chronic inflammatory diseases. We report the molecular basis of amyloidosis in a Korean girl who presented at 7 years of age with asymptomatic proteinuria and developed amyloid hep...

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Veröffentlicht in:	Kidney international 2005-11, Vol.68 (5), p.1994-1998
Hauptverfasser:	Gyung Kang, Hee, Bybee, Alison, Soo Ha, Il, Park, Moon Soo, Gilbertson, Janet A, Cheong, Hae Il, Choi, Yong, Hawkins, Philip N
Format:	Artikel
Sprache:	eng
Online-Zugang:	Volltext
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