Rare presentation of bardet-biedl syndrome as chronic liver disease with splenomegaly
Bardet-Biedl syndrome is a rare ciliopathic human autosomal-recessive disorder. It is a disorder that affects many parts of the body. Less than 15 cases have been reported from India. The signs and symptoms of this condition vary among affected individuals, even among members of the same family. It...
Saved in:
Main Authors: | J Manjula (Author), K Ravi (Author), V N Prashanth (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2020-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
BARDET-BIEDL SYNDROME - CASE PRESENTATION
by: Sorin Ioan Iurian, et al.
Published: (2015) -
Bardet Biedl syndrome - report of a very rare case
by: Asha Shirahatti, et al.
Published: (2016) -
Managing Bardet-Biedl Syndrome-Now and in the Future
by: Elizabeth Forsythe, et al.
Published: (2018) -
Bardet-Biedl syndrome with choledochal cyst: Rare association with a novel variant
by: Saket Kumar, et al.
Published: (2023) -
Bardet-Biedl syndrome and subaortic membrane: co-occurrence of two rare conditions
by: Osman Ziya Arık, et al.
Published: (2013)