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DOI 10.1002/ajmg.a.63128

Медицинская библиотека · American journal of medical genetics. Part A · 2023

Tethered cord syndrome in KBG syndrome.

Hills Sonia, Pugacheva Alisa, Weltin Patricia, Maughan Annette, Morton Sarah U, Feldman Henry A, Klinge Petra M, Agrawal Pankaj B

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Аннотация

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.

Для цитирования: Hills Sonia, Pugacheva Alisa, Weltin Patricia, Maughan Annette, Morton Sarah U, Feldman Henry A, Klinge Petra M, Agrawal Pankaj B. Tethered cord syndrome in KBG syndrome.. American journal of medical genetics. Part A. 2023. DOI: 10.1002/ajmg.a.63128.

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