Literature DB >> 8280889

Glutaric aciduria type II, an unusual cause of prenatal polycystic kidneys: report of prenatal diagnosis and confirmation of autosomal recessive inheritance.

A Hockey1, S Knowles, D Davies, W Carey, J Hurst, J Goldblatt.   

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Year:  1993        PMID： 8280889

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  3 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

2.  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

3.  A novel ETFB mutation in a patient with glutaric aciduria type II.

Authors:  Yosuke Sudo; Ayako Sasaki; Takashi Wakabayashi; Chikahiko Numakura; Kiyoshi Hayasaka
Journal:  Hum Genome Var       Date:  2015-06-18
  3 in total

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