Severe Hypocalcemia in the Adolescent as the Only Manifestation of <i>22q11</i> Microdeletion Syndrome: Clinical Case
Background. In this article, we would like to describe the atypical clinical picture and course of 22q11 microdeletion syndrome in a patient without specific phenotypic signs and symptoms typical for this disease.Clinical case description. Male patient, 13 years old, was hospitalized for the first t...
Saved in:
Main Authors: | Anastasia O. Vechkasova (Author), Natalia V. Buchinskaya (Author), Mikhail M. Kostik (Author) |
---|---|
Format: | Book |
Published: |
"Paediatrician" Publishers LLC,
2023-07-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Optimising immunisation in children with 22q11 microdeletion
by: Angela Berkhout, et al.
Published: (2020) -
Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland
by: Zeyland Joanna, et al.
Published: (2010) -
Speech Sounds Production, Narrative Skills, and Verbal Memory of Children with 22q11.2 Microdeletion
by: Marijana Rakonjac, et al.
Published: (2024) -
How Not to Miss the Mild Forms of Mucopolysaccharidosis Type I in Patients With Articular Manifestations of the Disease?
by: Natalia V. Buchinskaya, et al.
Published: (2019) -
Delayed diagnosis of 22q11 deletion syndrome due to late onset hypocalcemia in a 11-year-old girl with imperforated anus
by: Dong-Yoon Yoo, et al.
Published: (2017)