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Gazzetta Medica Italiana - Archivio per le Scienze Mediche 2019 October;178(10):838-42

DOI: 10.23736/S0393-3660.18.03884-6

Copyright © 2018 EDIZIONI MINERVA MEDICA

lingua: Inglese

A new case of M/SCHAD deficiency: the contribution of metabolic findings in directing the definitive genetic diagnosis for an optimal management

Alberto CASERTANO 1, Giulia FRISSO 2, 3, Giuseppe MONTEFUSCO 1, Cristina MAZZACCARA 2, 3, Guglielmo R. VILLANI 2, 3, Enza MOZZILLO 1 , Margherita RUOPPOLO 2, 3, Adriana FRANZESE 1

1 Section of Pediatrics, Department of Translational Medical Sciences, Federico II University, Naples, Italy; 2 Department of Molecular Medicine and Medical Biotechnology, Federico II University, Naples, Italy; 3 CEINGE Biotecnologie Avanzate Limited Liability Cooperative, Naples, Italy



Congenital hyperinsulinemic hypoglycemia (CHH) is a rare metabolic disease (prevalence <1/1,000,000) characterized by persistent hypoglycemia and inappropriate secretion of insulin often in neonatal period and infancy. Early diagnosis and management of patients with CHH are important to avoid brain damage. Recent advances in genetics have showed that CHH is due to mutations in twelve genes: ABCC8, KCNJ11, GCK, GLUD1, HADH, SLC16A1, UCP2, HNF1A, HNF4A, HK1, PGM1 and CACNA1D. The HADH gene codifies the medium and short chain 3-hydroxyacyl-CoA dehydrogenase (M/SCHAD), a mitochondrial matrix enzyme which catalyzes the penultimate reaction in the β-oxidation of medium and short-chain fatty acids, specifically the conversion of medium- and short-chain L-3-hydroxyacyl-CoA to corresponding 3-ketoacyl-CoA. Mutations in this gene result in a recessive form of CHH, with a good diazoxide responsivity and, occasionally, an abnormal urinary organic acid and plasma acylcarnitine’s profile. Herein, we describe a new case of CHH due to M/SCHAD deficiency, highlighting the importance of metabolic findings to lead genetic testing and clinical management.


KEY WORDS: Congenital hyperinsulinism; Diazoxide; Hypoglycemia

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