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Assessment of Growth in Cardio-Facio-Cutaneous Syndrome
Kari Johnston1, Sandesh C S Nagamani2,3, Bradley S Miller4
1School of Health Professions, Baylor College of Medicine, Houston, Texas, USA.
Insights
Individuals with Cardio-facio-cutaneous (CFC) syndrome exhibit persistent growth restriction from infancy to adulthood. Height Z-scores remain stable, while weight Z-scores progressively decline, indicating unique growth patterns in this rare disorder.
Area of Science:
- Genetics and Developmental Biology
- Pediatrics
- Endocrinology
Background:
- Cardio-facio-cutaneous (CFC) syndrome is a rare genetic disorder characterized by multiple congenital anomalies.
- Faltering growth is a common feature, but systematic growth parameter analysis is lacking.
Purpose of the Study:
- To systematically analyze growth parameters (height, weight, BMI) in individuals with CFC syndrome.
- To investigate the association of clinical factors with growth patterns in CFC syndrome.
Main Methods:
- Recruited 69 participants with CFC syndrome.
- Collected and analyzed height, weight, and BMI data.
- Compared Z-scores to a reference population.
Main Results:
- Individuals with CFC syndrome show consistently lower height-for-age and weight-for-age Z-scores.
- Growth restriction is evident from infancy through adulthood.
- Height Z-scores stabilize between -2 to -3 SD, while weight Z-scores progressively decrease over time.
- No significant differences in growth parameters were found based on enteral feeding, gene, or growth hormone deficiency status.
Conclusions:
- CFC syndrome is associated with significant and persistent growth restriction.
- Factors beyond feeding or growth hormone deficiency may influence growth, including malabsorption or hormonal resistance.
- Systematic growth assessment is crucial for identifying growth deviations and improving patient outcomes.
Abstract:
Cardio-facio-cutaneous (CFC) syndrome is a rare, multiple congenital anomaly disorder in which individuals commonly experience faltering growth; however, systematic analysis of growth parameters in this disorder has not been performed. We recruited 69 participants with CFC through CFC International and collected data on assessing height, weight, and body mass index (BMI). We found that the height-for-age and weight-for-age Z-scores were consistently lower in individuals with CFC than in the reference population and that children with CFC experience growth restriction from infancy to adulthood. Our findings show that as individuals age, their height Z-scores remain constant (-2 to -3 SD). However, over time, their weight shows a progressive decrease from average. There were no significant differences between the mean Z-scores of the growth parameters based on an individual's history of enteral feeding, gene associated with diagnosis, nor growth hormone deficiency status. This implies that feeding modality and severity of feeding difficulties may not be directly related to growth. Other factors could be responsible, such as malabsorption of nutrients, constitutional growth delay, hormonal deficiencies or resistance, or cardiac abnormalities. Our study is one of the first to systematically characterize growth parameters and analyze the association of clinical covariates with these parameters in individuals with CFC syndrome. Accurate assessment of growth in this rare condition will allow providers to recognize outliers of growth in their patients with CFC when compared to other individuals with CFC and make necessary referrals and recommendations, which may ultimately improve outcomes.
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