Literature DB >> 3754423

Glutaric acidemia type II. Phenotypic findings and ultrastructural studies of brain and kidney.

J C Harkin, W L Gill, E Shapira.   

Abstract

In a patient with nonketotic hypoglycemia, hyperammonemia, and a urinary organic acid pattern characteristic of glutaric acidemia type II, dysmorphic facial features and kidneys with multiple cortical cysts were the characteristic phenotypic findings. Electron microscopy revealed characteristic cytoplasmic, homogeneous, moderately electron-dense bodies with a limiting membrane. This specific lesion was noted in both central nervous system and renal tissues.

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Year:  1986        PMID: 3754423

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  8 in total

1.  Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities.

Authors:  Agnes Hackl; Katrin Mehler; Ingo Gottschalk; Anne Vierzig; Marcus Eydam; Jan Hauke; Bodo B Beck; Max C Liebau; Regina Ensenauer; Lutz T Weber; Sandra Habbig
Journal:  Pediatr Nephrol       Date:  2017-01-12       Impact factor: 3.714

Review 2.  Newborn screening and renal disease: where we have been; where we are now; where we are going.

Authors:  J Lawrence Merritt; David Askenazi; Si Houn Hahn
Journal:  Pediatr Nephrol       Date:  2011-09-27       Impact factor: 3.714

3.  Striatal degeneration in glutaric acidaemia type II.

Authors:  C W Chow; F E Frerman; S I Goodman; G K Brown; J J Pitt; D M Danks
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

Review 4.  Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes.

Authors:  C A Johnson; P Gissen; C Sergi
Journal:  J Med Genet       Date:  2003-05       Impact factor: 6.318

5.  Cardiomyopathy in multiple Acyl-CoA dehydrogenase deficiency: a clinico-pathological correlation and review of literature.

Authors:  Mohit Singla; Grace Guzman; Andrew J Griffin; Saroja Bharati
Journal:  Pediatr Cardiol       Date:  2007-10-03       Impact factor: 1.655

6.  Cystic renal dysplasia as a leading sign of inherited metabolic disease.

Authors:  Felix Distelmaier; Markus Vogel; Ute Spiekerkötter; Klaus Gempel; Dirk Klee; Stefan Braunstein; Heinz-Peter Groneck; Ertan Mayatepek; Udo Wendel; Bernd Schwahn
Journal:  Pediatr Nephrol       Date:  2007-07-19       Impact factor: 3.714

7.  Multi-organ abnormalities and mTORC1 activation in zebrafish model of multiple acyl-CoA dehydrogenase deficiency.

Authors:  Seok-Hyung Kim; Sarah A Scott; Michael J Bennett; Robert P Carson; Joshua Fessel; H Alex Brown; Kevin C Ess
Journal:  PLoS Genet       Date:  2013-06-13       Impact factor: 5.917

Review 8.  Glomerulocystic kidney disease.

Authors:  John J Bissler; Brian J Siroky; Hong Yin
Journal:  Pediatr Nephrol       Date:  2010-01-21       Impact factor: 3.714

  8 in total

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