Literature DB >> 742856

Carnitine deficiency: acute postpartum crisis.

C Angelini, E Govoni, M M Bragaglia, L Vergani.   

Abstract

A 16-year-old girl, previously in good health, developed progressive generalized muscle weakness following her first parturition. The neck and proximal limb muscles were especially weak and painful. Carnitine (4-trimethylamino-3-hydroxybutyrate) was markedly decreased in muscle, plasma, and urine. Dietary carnitine supplementation, 2.0 gm daily, was followed by clinical improvement and decreased lipid droplets in muscle biopsy. Together with previously reported cases, 2 fatal, the patient's illness emphasizes the risk of pregnancy in women with carnitine deficiency.

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Year:  1978        PMID: 742856     DOI: 10.1002/ana.410040616

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  8 in total

1.  Acute treatment-resistant post-partum necrotising myopathy with anti-Ro52/TRIM21 antibodies treated with rituximab.

Authors:  Savvas Psarelis; Doros Polydorou; Sophia Corsava; Constantinos Aristotelous
Journal:  Rheumatol Int       Date:  2015-01-08       Impact factor: 2.631

2.  Familial carnitine deficiency: further evidence for autosomal recessive transmission with variable expression.

Authors:  E Shahar; N Brand; Y Shapira; V Barash; A Gutman
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-02       Impact factor: 10.154

3.  Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathy.

Authors:  R C Sengers; J A Bakkeren; J M Trijbels; A M Stadhouders; G J Egberink; H J ter Laak; H J Jaspar
Journal:  Eur J Pediatr       Date:  1980-12       Impact factor: 3.183

4.  Influence of chain length of pyrene fatty acids on their uptake and metabolism by Epstein-Barr-virus-transformed lymphoid cell lines from a patient with multisystemic lipid storage myopathy and from control subjects.

Authors:  J Radom; R Salvayre; T Levade; L Douste-Blazy
Journal:  Biochem J       Date:  1990-07-01       Impact factor: 3.857

5.  Heterogeneous Phenotypes in Lipid Storage Myopathy Due to ETFDH Gene Mutations.

Authors:  Corrado Angelini; Daniela Tavian; Sara Missaglia
Journal:  JIMD Rep       Date:  2017-04-30

6.  Carnitine metabolism and inborn errors.

Authors:  A G Engel; C J Rebouche
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

7.  "Carnitine deficient" myopathy and cardiomyopathy with fatal outcome.

Authors:  F Cornelio; S Di Donato; D Testa; M Mora; G Gori; D Peluchetti; M Rimoldi
Journal:  Ital J Neurol Sci       Date:  1980-03

Review 8.  Carnitine in human nutrition.

Authors:  A C Bach
Journal:  Z Ernahrungswiss       Date:  1982-12
  8 in total

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