Arthrogryposis Congenita and Hepatorenal Abnormalities

J Gordon Millichap

doi:10.15844/pedneurbriefs-4-12-8

Arthrogryposis Congenita and Hepatorenal Abnormalities

Pediatric Neurology Briefs

Volume 4 (1990): Issue 12

By: J Gordon Millichap

Open Access

|Dec 1990

Abstract

Arthrogryposis multiplex congenita with renal and hepatic abnormalities, demonstrated at autopsy in a two month old child of consanguineous parents, is reported from the Pediatric Hospital, Coimbra, Portugal.

References

Saraiva JM Lemos C Gonçalves I Carneiro F Mota HC Arthrogryposis multiplex congenita with renal and hepatic abnormalities in a female infant J Pediatr 1990 Nov 117 5 761 3 10.1016/S0022-3476(05)83339-6 2231211
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Nezelof C Dupart MC Jaubert F Eliachar E A lethal familial syndrome associating arthrogryposis multiplex congenita, renal dysfunction, and a cholestatic and pigmentary liver disease J Pediatr 1979 Feb 94 2 258 60 10.1016/S0022-3476(79)80839-2 762621
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-4-12-8 | Journal eISSN: 2166-6482

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Language: English

Page range: 94 - 94

Published on: Dec 1, 1990

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Arthrogryposis Multiplex Congenita,

Metabolic Acidosis,

Electromyography

© 1990 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 4 (1990): Issue 12