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The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome

Feeding, eating and deglutition difficulties are key concerns in patients with cardiofaciocutaneous syndrome (CFCS). This study intends to quantify the development of feeding skills from birth to adulthood in patients with CFCS. Twenty-seven patients (eight males; mean age: 16.7 ± 8.3 years; median...

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Autores principales: Onesimo, Roberta, Sforza, Elisabetta, Giorgio, Valentina, Viscogliosi, Germana, Kuczynska, Eliza Maria, Margiotta, Gaia, Perri, Lucrezia, Limongelli, Domenico, Proli, Francesco, De Rose, Cristina, Rigante, Donato, Cerchiari, Antonella, Tartaglia, Marco, Leoni, Chiara, Zampino, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379052/
https://www.ncbi.nlm.nih.gov/pubmed/37510243
http://dx.doi.org/10.3390/genes14071338
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author Onesimo, Roberta
Sforza, Elisabetta
Giorgio, Valentina
Viscogliosi, Germana
Kuczynska, Eliza Maria
Margiotta, Gaia
Perri, Lucrezia
Limongelli, Domenico
Proli, Francesco
De Rose, Cristina
Rigante, Donato
Cerchiari, Antonella
Tartaglia, Marco
Leoni, Chiara
Zampino, Giuseppe
author_facet Onesimo, Roberta
Sforza, Elisabetta
Giorgio, Valentina
Viscogliosi, Germana
Kuczynska, Eliza Maria
Margiotta, Gaia
Perri, Lucrezia
Limongelli, Domenico
Proli, Francesco
De Rose, Cristina
Rigante, Donato
Cerchiari, Antonella
Tartaglia, Marco
Leoni, Chiara
Zampino, Giuseppe
author_sort Onesimo, Roberta
collection PubMed
description Feeding, eating and deglutition difficulties are key concerns in patients with cardiofaciocutaneous syndrome (CFCS). This study intends to quantify the development of feeding skills from birth to adulthood in patients with CFCS. Twenty-seven patients (eight males; mean age: 16.7 ± 8.3 years; median age: 15 years, age range: 1.5–38 years) with molecularly confirmed clinical diagnosis of CFCS were prospectively recruited from the Rare Disease Unit, Paediatrics Department, Fondazione Policlinico Agostino Gemelli-IRCCS, Rome, Italy, over a one-year period. Pathogenic variants along with key information regarding oro-motor features were collected. Sialorrhea was quantified using the Drooling Quotient 5. Feeding abilities were screened using the Italian version of the Montreal Children’s Hospital Feeding Scale (I-MCH-FS). The oral sensory processing section of the Sensory Profile completed the assessment. Mild-to-profuse drooling was experienced by 25% of patients, and food taste selectivity was a constant during infancy (65%), with persistence even beyond adolescence. Nineteen percent of participants with long-term enteral feeding dependency had BRAF, KRAS and MAP2K1 mutations. These findings document that mealtime challenges in CFCS do not remain restricted only to the paediatric age, and that supportive care until adulthood plays a key role.
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spelling pubmed-103790522023-07-29 The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome Onesimo, Roberta Sforza, Elisabetta Giorgio, Valentina Viscogliosi, Germana Kuczynska, Eliza Maria Margiotta, Gaia Perri, Lucrezia Limongelli, Domenico Proli, Francesco De Rose, Cristina Rigante, Donato Cerchiari, Antonella Tartaglia, Marco Leoni, Chiara Zampino, Giuseppe Genes (Basel) Article Feeding, eating and deglutition difficulties are key concerns in patients with cardiofaciocutaneous syndrome (CFCS). This study intends to quantify the development of feeding skills from birth to adulthood in patients with CFCS. Twenty-seven patients (eight males; mean age: 16.7 ± 8.3 years; median age: 15 years, age range: 1.5–38 years) with molecularly confirmed clinical diagnosis of CFCS were prospectively recruited from the Rare Disease Unit, Paediatrics Department, Fondazione Policlinico Agostino Gemelli-IRCCS, Rome, Italy, over a one-year period. Pathogenic variants along with key information regarding oro-motor features were collected. Sialorrhea was quantified using the Drooling Quotient 5. Feeding abilities were screened using the Italian version of the Montreal Children’s Hospital Feeding Scale (I-MCH-FS). The oral sensory processing section of the Sensory Profile completed the assessment. Mild-to-profuse drooling was experienced by 25% of patients, and food taste selectivity was a constant during infancy (65%), with persistence even beyond adolescence. Nineteen percent of participants with long-term enteral feeding dependency had BRAF, KRAS and MAP2K1 mutations. These findings document that mealtime challenges in CFCS do not remain restricted only to the paediatric age, and that supportive care until adulthood plays a key role. MDPI 2023-06-25 /pmc/articles/PMC10379052/ /pubmed/37510243 http://dx.doi.org/10.3390/genes14071338 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Onesimo, Roberta
Sforza, Elisabetta
Giorgio, Valentina
Viscogliosi, Germana
Kuczynska, Eliza Maria
Margiotta, Gaia
Perri, Lucrezia
Limongelli, Domenico
Proli, Francesco
De Rose, Cristina
Rigante, Donato
Cerchiari, Antonella
Tartaglia, Marco
Leoni, Chiara
Zampino, Giuseppe
The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome
title The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome
title_full The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome
title_fullStr The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome
title_full_unstemmed The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome
title_short The “FEEDS (FEeding Eating Deglutition Skills)” over Time Study in Cardiofaciocutaneous Syndrome
title_sort “feeds (feeding eating deglutition skills)” over time study in cardiofaciocutaneous syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379052/
https://www.ncbi.nlm.nih.gov/pubmed/37510243
http://dx.doi.org/10.3390/genes14071338
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