A case report of Omenn syndrome in siblings
The article describes a case of Omenn syndrome in neonatal period. Omenn syndrome was diagnosed in two of three children of the same parents. Both of children had skin erythroderma since birth and eosynophilia in blood tests. The course of the disease in both cases was fatal. Condition has inborn ch...
Saved in:
Main Authors: | Agnieszka Berendt (Author), Monika Wójtowicz-Marzec (Author), Monika Dobrowolska (Author), Anna Kwaśniewska (Author) |
---|---|
Format: | Book |
Published: |
Kazimierz Wielki University,
2019-05-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
A case report of Omenn syndrome in siblings
by: Agnieszka Berendt, et al.
Published: (2019) -
Severe haemophilia A in a preterm girl with Turner syndrome: case report - a diagnostic and therapeutic challenge for a paediatrician (Part 2)
by: Berendt Agnieszka, et al.
Published: (2021) -
Severe haemophilia a in a preterm girl with turner syndrome - a case report from the prenatal period to early infancy (part I)
by: Agnieszka Berendt, et al.
Published: (2020) -
Omenn syndrome: a case report and review of literature
by: Chia-Chi Hsu, et al.
Published: (2011) -
Prenatal diagnosis of urinary track defects
by: Agnieszka Maria Berendt, et al.
Published: (2019)