Sanjad-Sakati syndrome with corneal opacity in a Palestinian neonate: case report
Sanjad-Sakati syndrome is an autosomal recessive disorder found mainly in people of Arabian origin. This is a report of a Palestinian premature (35 weeks gestation) newborn who was part of twins and had this rare disease. The syndrome comprises congenital hypoparathyroidism, hypocalcaemia, seizure,...
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Book |
| Published: |
Hygeia Press di Corridori Marinella,
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!
|
Internet
Connect to this object online.3rd Floor Main Library
| Call Number: |
A1234.567 |
|---|---|
| Copy 1 | Available |