Arthrogryposis Congenita and Hepatorenal Abnormalities
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.
Saved in:
Main Author: | J Gordon Millichap (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1990-12-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Arthrogryposis Multiplex Congenita: Case Report
by: Ayla Aktulay, et al.
Published: (2016) -
Congenital Brachial Arthrogryposis
by: J Gordon Millichap
Published: (1993) -
Spinal Muscular Atrophy and Arthrogryposis
by: J Gordon Millichap
Published: (1997) -
Congenital Arthrogryposis and Maternal Myasthenia
by: J Gordon Millichap
Published: (1988) -
Arthrogryposis multiplex congenita with maxillofacial involvement: a case report
by: Stefano Cirillo, et al.
Published: (2023)