Fanconi-Bickel syndrome presenting in neonatal screening for galactosaemia
J Inherit Metab Dis
.
1997 Aug;20(4):607-8.
doi: 10.1023/a:1005375629820.
Authors
D Müller
1
,
R Santer
,
M Krawinkel
,
B Christiansen
,
J Schaub
Affiliation
1
University Children's Hospital, Kiel, Germany.
PMID:
9266402
DOI:
10.1023/a:1005375629820
No abstract available
Publication types
Case Reports
MeSH terms
Fanconi Syndrome / diagnosis*
Female
Galactosemias / diagnosis*
Glycogen Storage Disease / diagnosis*
Humans
Infant
Infant, Newborn
Male
Neonatal Screening