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Journal articles on the topic 'Inborn errors of metabolism'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2024

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1

BURTON, BARBARA K. "Inborn Errors of Metabolism." Pediatrics 80, no. 4 (October 1, 1987): 600. http://dx.doi.org/10.1542/peds.80.4.600.

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In Reply.— I thank Drs Wiswell and Weisse for their interesting observations regarding the occurrence of intracranial hemorrhage in term infants with inborn errors of metabolism. There is no question that intracranial hemorrhage is a potentially devastating, although presumably uncommon, complication of these disorders. In my personal experience, neonates with inborn errors of metabolism who have experienced intracranial hemorrhages have all had obvious predisposing factors, such as severe metabolic acidosis, which would provide a clue to the underlying diagnosis.

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2

Levy, Paul A. "Inborn Errors of Metabolism." Pediatrics In Review 30, no. 4 (April 1, 2009): e22-e28. http://dx.doi.org/10.1542/pir.30.4.e22.

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3

WISWELL, THOMAS E., and MARTIN E. WEISSE. "Inborn Errors of Metabolism." Pediatrics 80, no. 4 (October 1, 1987): 599–600. http://dx.doi.org/10.1542/peds.80.4.599.

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To the Editor.— We read with great interest the review by Dr Burton on inborn errors of metabolism.1 These myriad disorders frequently present with clinical manifestations that are associated with a variety of more common neonatal diseases. Dr Burton is to be commended for presenting a lucid, rational approach for the diagnosis of these oft-confusing afflictions. However, there is another manifestation of these disorders, not previously recognized in the pediatric literature, that we wish to address.

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4

Levy, Paul A. "Inborn Errors of Metabolism." Pediatrics In Review 30, no. 4 (April 1, 2009): 131–38. http://dx.doi.org/10.1542/pir.30.4.131.

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5

Kiess, Wieland, Anna Kirstein, and Skadi Beblo. "Inborn errors of metabolism." Journal of Pediatric Endocrinology and Metabolism 33, no. 1 (January 28, 2020): 1–3. http://dx.doi.org/10.1515/jpem-2019-0582.

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6

Berry, Helen K. "Inborn Errors of Metabolism." Endocrinologist 2, no. 4 (July 1992): 276–77. http://dx.doi.org/10.1097/00019616-199207000-00011.

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7

Waber, Lewis. "Inborn Errors of Metabolism." Pediatric Annals 19, no. 2 (February 1, 1990): 105–18. http://dx.doi.org/10.3928/0090-4481-19900201-08.

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8

Giugliani, Roberto, Carlos S. Dutra-Filho, Maria L. Barth, Janice C. Dutra, Moacir Wajner, Clovis M. D. Wannmacher, and Lenir T. Montagner. "Inborn Errors of Metabolism." Clinical Pediatrics 28, no. 11 (November 1989): 494–97. http://dx.doi.org/10.1177/000992288902801101.

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9

Nyhan, William L., and Deborah L. Marsden. "Inborn errors of metabolism." Current Opinion in Pediatrics 2, no. 4 (August 1990): 749–52. http://dx.doi.org/10.1097/00008480-199008000-00022.

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10

Molleston, Jean P., and David H. Perlmutter. "Inborn errors of metabolism." Current Opinion in Pediatrics 4, no. 5 (October 1992): 798–804. http://dx.doi.org/10.1097/00008480-199210000-00012.

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11

El-Hattab, Ayman W., and V. Reid Sutton. "Inborn Errors of Metabolism." Pediatric Clinics of North America 65, no. 2 (April 2018): i. http://dx.doi.org/10.1016/s0031-3955(18)30012-9.

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12

Saudubray, J. M. "Inborn errors of metabolism." Seminars in Neonatology 7, no. 1 (February 2002): 1. http://dx.doi.org/10.1053/siny.2001.0082.

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13

Sawley, Linda. "Inborn errors of metabolism." Paediatric Nursing 10, no. 5 (June 1998): 25–27. http://dx.doi.org/10.7748/paed.10.5.25.s21.

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14

El-Hattab, Ayman W. "Inborn Errors of Metabolism." Clinics in Perinatology 42, no. 2 (June 2015): 413–39. http://dx.doi.org/10.1016/j.clp.2015.02.010.

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15

Vernon, Hilary J. "Inborn Errors of Metabolism." JAMA Pediatrics 169, no. 8 (August 1, 2015): 778. http://dx.doi.org/10.1001/jamapediatrics.2015.0754.

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16

Almannai, Mohammed, Majid Alfadhel, and Ayman W. El-Hattab. "Carnitine Inborn Errors of Metabolism." Molecules 24, no. 18 (September 6, 2019): 3251. http://dx.doi.org/10.3390/molecules24183251.

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Carnitine plays essential roles in intermediary metabolism. In non-vegetarians, most of carnitine sources (~75%) are obtained from diet whereas endogenous synthesis accounts for around 25%. Renal carnitine reabsorption along with dietary intake and endogenous production maintain carnitine homeostasis. The precursors for carnitine biosynthesis are lysine and methionine. The biosynthetic pathway involves four enzymes: 6-N-trimethyllysine dioxygenase (TMLD), 3-hydroxy-6-N-trimethyllysine aldolase (HTMLA), 4-N-trimethylaminobutyraldehyde dehydrogenase (TMABADH), and γ-butyrobetaine dioxygenase (BBD). OCTN2 (organic cation/carnitine transporter novel type 2) transports carnitine into the cells. One of the major functions of carnitine is shuttling long-chain fatty acids across the mitochondrial membrane from the cytosol into the mitochondrial matrix for β-oxidation. This transport is achieved by mitochondrial carnitine–acylcarnitine cycle, which consists of three enzymes: carnitine palmitoyltransferase I (CPT I), carnitine-acylcarnitine translocase (CACT), and carnitine palmitoyltransferase II (CPT II). Carnitine inborn errors of metabolism could result from defects in carnitine biosynthesis, carnitine transport, or mitochondrial carnitine–acylcarnitine cycle. The presentation of these disorders is variable but common findings include hypoketotic hypoglycemia, cardio(myopathy), and liver disease. In this review, the metabolism and homeostasis of carnitine are discussed. Then we present details of different inborn errors of carnitine metabolism, including clinical presentation, diagnosis, and treatment options. At the end, we discuss some of the causes of secondary carnitine deficiency.

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17

Lennard, Martin S., Geoffrey T. Tucker, and H. Frank Woods. "Inborn ???Errors??? of Drug Metabolism." Clinical Pharmacokinetics 19, no. 4 (October 1990): 257–63. http://dx.doi.org/10.2165/00003088-199019040-00001.

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18

MacFarlane, A. W. "Inborn errors of lipid metabolism." Clinical and Experimental Dermatology 14, no. 4 (July 1989): 334. http://dx.doi.org/10.1111/j.1365-2230.1989.tb02004.x.

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19

Blau, N. "Inborn Errors of Pterin Metabolism." Annual Review of Nutrition 8, no. 1 (July 1988): 185–209. http://dx.doi.org/10.1146/annurev.nu.08.070188.001153.

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20

Van den Berghe, Georges. "Inborn Errors of Fructose Metabolism." Annual Review of Nutrition 14, no. 1 (July 1994): 41–58. http://dx.doi.org/10.1146/annurev.nu.14.070194.000353.

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21

Worwood, M. "Inborn errors of metabolism: iron." British Medical Bulletin 55, no. 3 (January 1, 1999): 556–67. http://dx.doi.org/10.1258/0007142991902628.

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22

Hommes, F. A. "Inborn errors of fructose metabolism." American Journal of Clinical Nutrition 58, no. 5 (November 1, 1993): 788S—795S. http://dx.doi.org/10.1093/ajcn/58.5.788s.

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23

Saudubray, Jean-Marie, and Àngels Garcia-Cazorla. "Inborn Errors of Metabolism Overview." Pediatric Clinics of North America 65, no. 2 (April 2018): 179–208. http://dx.doi.org/10.1016/j.pcl.2017.11.002.

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24

Mitsubuchi, Hiroshi, Kimitoshi Nakamura, Shiro Matsumoto, and Fumio Endo. "Inborn Errors of Proline Metabolism." Journal of Nutrition 138, no. 10 (October 1, 2008): 2016S—2020S. http://dx.doi.org/10.1093/jn/138.10.2016s.

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25

Leonard, J. V. "Teratogenic inborn errors of metabolism." Postgraduate Medical Journal 62, no. 724 (February 1, 1986): 125–29. http://dx.doi.org/10.1136/pgmj.62.724.125.

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26

Mayatepek, Ertan, Björn Hoffmann, and Thomas Meissner. "Inborn errors of carbohydrate metabolism." Best Practice & Research Clinical Gastroenterology 24, no. 5 (October 2010): 607–18. http://dx.doi.org/10.1016/j.bpg.2010.07.012.

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27

Nyhan, W. L. "Inborn errors of biotin metabolism." Archives of Dermatology 123, no. 12 (December 1, 1987): 1696–98. http://dx.doi.org/10.1001/archderm.123.12.1696.

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28

Gibson, Kenneth M., William L. Nyhan, and Jaak Jaeken. "Inborn errors of GABA metabolism." BioEssays 4, no. 1 (January 1986): 24–27. http://dx.doi.org/10.1002/bies.950040107.

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29

Nyhan, William L. "Inborn Errors of Biotin Metabolism." Archives of Dermatology 123, no. 12 (December 1, 1987): 1696. http://dx.doi.org/10.1001/archderm.1987.01660360146027.

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30

Lodh, Moushumi, and Joshi Anand Kerketta. "Citrullinemia and Hyperglycinemia Presenting with Seizures - Case Report of a 4 Day Old Baby." Asian Journal of Medical Sciences 3, no. 1 (February 18, 2013): 17–20. http://dx.doi.org/10.3126/ajms.v3i1.4801.

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Inborn errors of amino acid metabolism (IEM) are of concern in India, the spectrum being wide, varied and poorly diagnosed. Since aggregate incidence of inborn errors of metabolism is relatively high, in countries such as India, a high degree of suspicion is essential to correctly diagnose an inborn error of amino acid metabolism. We report a case of citrullinemia, glycinemia with hyperammonaemia and seizures in a 4-dayold previously asymptomatic baby, with a brief review of the literature. DOI: http://dx.doi.org/10.3126/ajms.v3i1.4801 Asian Journal of Medical Sciences 3(2012) 17-20

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31

MP, Narayanan. "Inborn Errors of Metabolism: Indian Scenario." Acta Scientific Paediatrics 2, no. 11 (October 22, 2019): 50–52. http://dx.doi.org/10.31080/aspe.2019.02.0169.

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32

Rice, G. M., and R. D. Steiner. "Inborn Errors of Metabolism (Metabolic Disorders)." Pediatrics in Review 37, no. 1 (January 1, 2016): 3–17. http://dx.doi.org/10.1542/pir.2014-0122.

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33

Belousova, E. D. "EPILEPSY IN INBORN ERRORS OF METABOLISM." Epilepsia and paroxyzmal conditions 8, no. 1 (January 1, 2016): 55–61. http://dx.doi.org/10.17749/2077-8333.2016.8.1.055-061.

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34

RAHMAN, SHAMIMA, EMMA J. FOOTITT, SOPHIA VARADKAR, and PETER T. CLAYTON. "Inborn errors of metabolism causing epilepsy." Developmental Medicine & Child Neurology 55, no. 1 (September 24, 2012): 23–36. http://dx.doi.org/10.1111/j.1469-8749.2012.04406.x.

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35

Fukao, Toshiyuki, and Kimitoshi Nakamura. "Advances in inborn errors of metabolism." Journal of Human Genetics 64, no. 2 (January 25, 2019): 65. http://dx.doi.org/10.1038/s10038-018-0535-7.

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36

Kwon, Jennifer M. "Testing for Inborn Errors of Metabolism." CONTINUUM: Lifelong Learning in Neurology 24, no. 1 (February 2018): 37–56. http://dx.doi.org/10.1212/con.0000000000000563.

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37

Kimonis, Virginia. "Dysmorphology of inborn errors of metabolism." Molecular Cytogenetics 7, Suppl 1 (2014): I39. http://dx.doi.org/10.1186/1755-8166-7-s1-i39.

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38

Jalan, Anil B. "Treatment of inborn errors of metabolism." Molecular Cytogenetics 7, Suppl 1 (2014): I42. http://dx.doi.org/10.1186/1755-8166-7-s1-i42.

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39

Walter, J. H. "Inborn errors of metabolism and pregnancy." Journal of Inherited Metabolic Disease 23, no. 3 (May 2000): 229–36. http://dx.doi.org/10.1023/a:1005679928521.

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40

Velázquez, Antonio, Marcela Vela-Amieva, Isabel Cicerón-Arellano, Isabel Ibarra-González, Martha Elva Pérez-Andrade, Zazil Olivares-Sandoval, and Gerardo Jiménez-Sánchez. "Diagnosis of Inborn Errors of Metabolism." Archives of Medical Research 31, no. 2 (March 2000): 145–50. http://dx.doi.org/10.1016/s0188-4409(00)00053-9.

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41

Schillaci, Lori-Anne P., Suzanne D. DeBrosse, and Shawn E. McCandless. "Inborn Errors of Metabolism with Acidosis." Pediatric Clinics of North America 65, no. 2 (April 2018): 209–30. http://dx.doi.org/10.1016/j.pcl.2017.11.003.

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42

Summar, Marshall L., and Nicholas Ah Mew. "Inborn Errors of Metabolism with Hyperammonemia." Pediatric Clinics of North America 65, no. 2 (April 2018): 231–46. http://dx.doi.org/10.1016/j.pcl.2017.11.004.

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43

Weinstein, David A., Ulrike Steuerwald, Carolina F. M. De Souza, and Terry G. J. Derks. "Inborn Errors of Metabolism with Hypoglycemia." Pediatric Clinics of North America 65, no. 2 (April 2018): 247–65. http://dx.doi.org/10.1016/j.pcl.2017.11.005.

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44

El-Gharbawy, Areeg, and Jerry Vockley. "Inborn Errors of Metabolism with Myopathy." Pediatric Clinics of North America 65, no. 2 (April 2018): 317–35. http://dx.doi.org/10.1016/j.pcl.2017.11.006.

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45

Almannai, Mohammed, and Ayman W. El-Hattab. "Inborn Errors of Metabolism with Seizures." Pediatric Clinics of North America 65, no. 2 (April 2018): 279–99. http://dx.doi.org/10.1016/j.pcl.2017.11.007.

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46

Demirbas, Didem, William J. Brucker, and Gerard T. Berry. "Inborn Errors of Metabolism with Hepatopathy." Pediatric Clinics of North America 65, no. 2 (April 2018): 337–52. http://dx.doi.org/10.1016/j.pcl.2017.11.008.

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47

Dulac, O. "Epilepsy in inborn errors of metabolism." European Journal of Paediatric Neurology 12 (May 2008): S1. http://dx.doi.org/10.1016/s1090-3798(08)70006-0.

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48

Pollitt, Rodney J., and Mark J. Sharrard. "Treating rare inborn errors of metabolism." Lancet 364, no. 9452 (December 2004): 2158–60. http://dx.doi.org/10.1016/s0140-6736(04)17606-x.

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49

Mitchell, Beverly S. "C01 Inborn errors of purine metabolism." Nutrition Clinique et Métabolisme 6, no. 4 (January 1992): 241. http://dx.doi.org/10.1016/s0985-0562(05)80376-0.

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50

Poll-Thé, B. T. "Inborn errors of metabolism and seizures." Clinical Neurology and Neurosurgery 93, no. 4 (January 1991): 348. http://dx.doi.org/10.1016/0303-8467(91)90105-x.

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