Back to Search Start Over

Tethered cord syndrome in KBG syndrome.

Authors :
Hills, Sonia
Pugacheva, Alisa
Weltin, Patricia
Maughan, Annette
Morton, Sarah U.
Feldman, Henry A.
Klinge, Petra M.
Agrawal, Pankaj B.
Source :
American Journal of Medical Genetics. Part A; May2023, Vol. 191 Issue 5, p1222-1226, 5p
Publication Year :
2023

Abstract

Tethered cord syndrome (TCS) is characterized by leg pain and weakness, bladder and bowel dysfunction, orthopedic malformations such as scoliosis, and motor deficits caused by the fixation of the spinal cord to surrounding tissues. TCS is surgically treatable and often found in conjunction with other syndromic conditions. KBG syndrome is caused by variants in the ANKRD11 gene and is characterized by short stature, developmental delay, macrodontia, and a triangular face. The current study explores the prevalence of TCS in pediatric KBG patients and their associated signs and symptoms. Patients with KBG were surveyed for signs and symptoms associated with TCS and asked if they had been diagnosed with the syndrome. We found a high proportion of patients diagnosed with (11%) or being investigated for TCS (24%), emphasizing the need to further characterize the comorbid syndromes. No signs or symptoms clearly emerged as indicative of TCS in KBG patients, but some the prevalence of some signs and symptoms varied by sex. Male KBG patients with diagnosed TCS were more likely to have coordination issues and global delay/brain fog than their female counterparts. Understanding the presentation of TCS in KBG patients is critical for timely diagnosis and treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15524825
Volume :
191
Issue :
5
Database :
Complementary Index
Journal :
American Journal of Medical Genetics. Part A
Publication Type :
Academic Journal
Accession number :
162971768
Full Text :
https://doi.org/10.1002/ajmg.a.63128