Harlequin fetus: A case report
Harlequin ichthyosis (HI) is the most severe type of congenital ichthyosis. It is extremely rare with very few cases reported in India. It is inherited in an autosomal recessive fashion. The importance of antenatal diagnosis by ultrasonography, DNA-based molecular studies on chorionic villus samplin...
Saved in:
Main Authors: | Mangesh Machindra Londhe (Author), Tushar Vitthalrao Patil (Author), Kishor Hiraman Suryawanshi (Author) |
---|---|
Format: | Book |
Published: |
Wolters Kluwer Medknow Publications,
2022-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Harlequin Fetus
by: Sengupta B, et al.
Published: (1995) -
Harlequin fetus in a twin sibling: a rare case report
by: Rabia Merve Palalıoğlu, et al.
Published: (2021) -
Prenatal diagnose of a fetus with Harlequin ichthyosis in a Chinese family
by: Wei Jian, et al.
Published: (2018) -
Harlequin Ichthyosis: Case Report
by: Patrícia A. Couto, et al.
Published: (2019) -
Harlequin Ichtyosis: A Case Report
by: Yetkin Karasu, et al.
Published: (2009)