Publications by authors named "H A Lemonde"

Since the UK commenced newborn screening for isovaleric acidemia in 2015, changes in prescribing have increased the incidence of false positive (FP) results due to pivaloylcarnitine. A review of screening results between 2015 and 2022 identified 24 true positive (TP) and 84 FP cases, with pivalate interference confirmed in 76/84. Initial C5 carnitine (C5C) did not discriminate between FP and TP with median (range) C5C of 2.

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Ornithine transcarbamylase deficiency (OTCD) is an X-linked defect of ureagenesis and the most common urea cycle disorder. Patients present with hyperammonemia causing neurological symptoms, which can lead to coma and death. Liver transplantation (LT) is the only curative therapy, but has several limitations including organ shortage, significant morbidity and requirement of lifelong immunosuppression.

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Analysis of blood phenylalanine is central to the monitoring of patients with phenylketonuria (PKU) and age-related phenylalanine target treatment-ranges (0-12 years; 120-360 μmol/L, and >12 years; 120-600 μmol/L) are recommended in order to prevent adverse neurological outcomes. These target treatment-ranges are based upon plasma phenylalanine concentrations. However, patients are routinely monitored using dried bloodspot (DBS) specimens due to the convenience of collection.

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Article Synopsis
  • Isolated complex I deficiency is a common issue in pediatric mitochondrial diseases linked to genetic mutations in complex I genes, affecting its structure and function.
  • Next-generation sequencing has helped diagnose four unrelated children with symptoms suggestive of mitochondrial disorders, identifying bi-allelic variants in the NDUFA6 gene, which plays a key role in complex I assembly.
  • Functional tests revealed that the mutations led to defects in complex I assembly in patients' fibroblast cells, but using lentiviral transduction restored normal function, also indicating the formation of a supercomplex with other mitochondrial complexes.
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The vitamin B status of infants depends on maternal B status during pregnancy, and during lactation if breastfed. We present a 9-month-old girl who was admitted to the metabolic unit for assessment of developmental delay. She was exclusively breastfed and the introduction of solids at 5 months was unsuccessful.

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