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Summary
INFANTILE LIVER FAILURE SYNDROME 1 (ILFS1, LARS)
INFANTILE LIVER FAILURE SYNDROME 1 ILFS1
615438
OMIM = Online Medalian Inheritance of Men
370088
5q32
rare (6 families)
autosomal recessive
mutation in the LARS gene
symptoms
aminoaciduria
anemia
Coagulopathy/Coagulation factors
developmental delay
failure to thrive
hepatomegaly (large liver)
hyperammonemia
hypotonia
intrauterine growth retardation
lactic acidosis
liver failure
microcephaly (<2 SD for age)
onset, infancy
onset, neonatal
renal dysfunction, renal defects
seizures
vomiting
laboratory finding
Ammonia0.000.00 +€mol/lblood
L-Lactic acid mmol/lplasma
MRI, brain, abnormalities -
Albumin g/lplasma
4-Hydroxyphenylpyruvic acid mmol/mol Creaurine
4-Hydroxyphenyllactic acid mmol/mol Creaurine
Literature
Tazawa Yet al.Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patientsMol Genet Metab830213-2192004
Schenk Bet al.MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type IfJ Clin Invest11161687-16952003
Velho RV,et al.A de novo or germline mutation in a family with Mucolipidosis III gamma: Implications for molecular diagnosis and genetic counselingMol Genet Metab Rep1098-1022014
Njajou OT,et al.A mutation in SLC11A3 is associated with autosomal dominant hemochromatosisNat Genet283213-2142001
Varun S,Kiruba Daniel SC, Gorthi SSRapid sensing of melamine in milk by interference green synthesis of silver nanoparticlesMater Sci Eng C Mater Biol Appl740253-2582017
Hachisu Met al.Citrin deficiency presenting with ketotic hypoglycaemia and hepatomegaly in childhoodEur J Pediatr1642109-1102005