Argininosuccinate lyase deficiency: longterm outcome of 13 patients detected by newborn screening. 2009

C Ficicioglu, and R Mandell, and V E Shih
Massachusetts General Hospital, Amino Acid Disorders Laboratory, Boston, MA 02114, USA.

Argininosuccinate lyase deficiency is a urea cycle disorder which can present in the neonatal period with hyperammonemic encephalopathy, or later in childhood with episodic vomiting, growth and developmental delay. Abnormal hair, hepatomegaly, and hepatic fibrosis are unique features of this disorder. Twelve patients with argininosuccinate lyase deficiency were ascertained between 4 and 6 weeks of age by urine amino acid screening. One infant in a previously identified family was diagnosed shortly after birth. Diagnosis was confirmed by enzyme assay in red blood cells and/or skin fibroblasts. At the time of last follow-up, patients had been followed for 13-33 years. All patients were asymptomatic at detection, 7 had slightly increased blood ammonia, and all were initially treated with low-protein diet. Utilization of (14)C-citrulline by intact skin fibroblasts measured by (14)C incorporation into macromolecules was 74-135% of the control mean for 7 of the 8 patients studied. Nine patients had normal development, 4 had learning disability, 6 had EEG abnormalities, 3 had seizure disorder. None had any episodes of hyperammonemic coma. None had hepatomegaly. Patients detected by screening had higher enzyme activity measured by the (14)C-citrulline incorporation assay than comparison groups of patients with neonatal-onset and with late-onset detected by clinical disease. The ability to utilize (14)C-citrulline by intact fibroblasts seems to correlate with clinical outcome and may have prognostic value. It is likely that early diagnosis and treatment contributed to the relatively mild clinical course of the study group.

UI MeSH Term Description Entries
D007223 Infant A child between 1 and 23 months of age. Infants
D007231 Infant, Newborn An infant during the first 28 days after birth. Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D002956 Citrulline
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D001123 Argininosuccinate Lyase An enzyme of the urea cycle which splits argininosuccinate to fumarate plus arginine. Its absence leads to the metabolic disease ARGININOSUCCINIC ACIDURIA in man. EC 4.3.2.1. Argininosuccinase,Lyase, Argininosuccinate
D015997 Neonatal Screening The identification of selected parameters in newborn infants by various tests, examinations, or other procedures. Screening may be performed by clinical or laboratory measures. A screening test is designed to sort out healthy neonates (INFANT, NEWBORN) from those not well, but the screening test is not intended as a diagnostic device, rather instead as epidemiologic. Infant, Newborn, Screening,Newborn Infant Screening,Newborn Screening,Neonatal Screenings,Newborn Infant Screenings,Newborn Screenings,Screening, Neonatal,Screening, Newborn,Screening, Newborn Infant,Screenings, Neonatal,Screenings, Newborn,Screenings, Newborn Infant
D056807 Argininosuccinic Aciduria Rare autosomal recessive disorder of the urea cycle which leads to the accumulation of argininosuccinic acid in body fluids and severe HYPERAMMONEMIA. Clinical features of the neonatal onset of the disorder include poor feeding, vomiting, lethargy, seizures, tachypnea, coma, and death. Later onset results in milder set of clinical features including vomiting, failure to thrive, irritability, behavioral problems, or psychomotor retardation. Mutations in the ARGININOSUCCINATE LYASE gene cause the disorder. Arginino Succinase Deficiency,ASA Deficiency,ASL Deficiency,Argininosuccinase Deficiency,Argininosuccinate Acidemia,Argininosuccinate Lyase Deficiency,Argininosuccinic Acid Lyase Deficiency,Argininosuccinic Acidemia,Argininosuccinicaciduria,Argininosuccinyl-Coa Lyase Deficiency,Arginosuccinase Deficiency,Asauria,Inborn Error of Urea Synthesis, Arginino Succinic Type,Urea Cycle Disorder, Arginino Succinase Type,ASA Deficiencies,ASL Deficiencies,Acidemia, Argininosuccinate,Acidemias, Argininosuccinate,Aciduria, Argininosuccinic,Acidurias, Argininosuccinic,Arginino Succinase Deficiencies,Argininosuccinate Acidemias,Argininosuccinate Lyase Deficiencies,Argininosuccinic Acidurias,Argininosuccinicacidurias,Deficiencies, ASA,Deficiencies, ASL,Deficiencies, Arginino Succinase,Deficiencies, Argininosuccinate Lyase,Deficiency, ASA,Deficiency, ASL,Deficiency, Arginino Succinase,Deficiency, Argininosuccinate Lyase

Related Publications

C Ficicioglu, and R Mandell, and V E Shih
May 2010, Molecular genetics and metabolism,
C Ficicioglu, and R Mandell, and V E Shih
January 1998, Ryoikibetsu shokogun shirizu,
C Ficicioglu, and R Mandell, and V E Shih
May 2012, Genetics in medicine : official journal of the American College of Medical Genetics,
C Ficicioglu, and R Mandell, and V E Shih
April 1999, Journal of inherited metabolic disease,
C Ficicioglu, and R Mandell, and V E Shih
August 1988, Acta paediatrica Japonica : Overseas edition,
C Ficicioglu, and R Mandell, and V E Shih
July 1990, The Journal of pediatrics,
C Ficicioglu, and R Mandell, and V E Shih
January 2023, Indian journal of dermatology, venereology and leprology,
C Ficicioglu, and R Mandell, and V E Shih
February 1993, The Journal of pediatrics,
C Ficicioglu, and R Mandell, and V E Shih
October 2008, Human genetics,
C Ficicioglu, and R Mandell, and V E Shih
October 2008, Human genetics,
Copied contents to your clipboard!