Journal Article

Growth in ataxia telangiectasia

Natale, Valerie A. I., Rothblum-Oviatt, Cynthia, Schlechter, Haley, McGrath-Morrow, Sharon A., Lefton-Greif, Maureen A., Cole, Tim J., Wright, Jennifer, Crawford, Thomas O., Lederman, Howard M.

2021

Overview

Background Ataxia telangiectasia (A-T) is a DNA repair disorder that affects multiple body systems. Neurological problems and immunodeficiency are two important features of this disease. At this time, two main severity groups are defined in A-T: classic (the more severe form) and mild. Poor growth is a common problem in classic A-T. An objective of this study was to develop growth references for classic A-T. Another objective was to compare growth patterns in classic A-T and mild A-T with each other and with the general population, using the CDC growth references. A final objective was to examine the effects of chronic infection on height. Results We found that classic A-T patients were smaller overall, and suffered from height and weight faltering that continued throughout childhood and adolescence. When compared to the CDC growth references, the median heights and weights for both male and female patients eventually fell to or below the 3rd centile on the CDC charts. Height faltering was more pronounced in females. Birthweight was lower in the classic A-T group compared to mild A-T and the general population, whereas birth length was not. Finally, we investigated height and BMI faltering in relation to number of infections and found no association. Conclusions Classic A-T appears to affect growth in utero. Although children appear to grow well in very early life, faltering begins early, and is unrelenting.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Adolescent / Age / Ataxia / Ataxia Telangiectasia / Birth weight / Body Height / Body Weight / Child / Children / Chronic infection / Complications and side effects / Datasets / Diabetes / DNA repair / Expected values / Female / Females / Growth / Growth charts / Growth Disorders / Growth patterns / Human Genetics / Humans / Immunodeficiency / Infections / Kinases / Male / Medical records / Medical research / Medicine / Medicine & Public Health / Mutation / Patients / Pediatric research / Pharmacology/Toxicology / Population / Proteins / Rare diseases / Rare neurological diseases / Risk factors