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

Author:

Onesimo Roberta1ORCID,Sforza Elisabetta2ORCID,Giorgio Valentina12ORCID,Viscogliosi Germana1ORCID,Kuczynska Eliza Maria1,Margiotta Gaia1,Perri Lucrezia1,Limongelli Domenico1,Proli Francesco1,De Rose Cristina1,Rigante Donato12ORCID,Cerchiari Antonella3,Tartaglia Marco4ORCID,Leoni Chiara1ORCID,Zampino Giuseppe12

Affiliation:

1. Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Italy

2. Dipartimento Scienze della Vita e Sanità Pubblica, Facoltà di Medicina e Chirurgia, Università Cattolica del S. Cuore, 00168 Rome, Italy

3. Feeding and Swallowing Services Unit, Department of Neuroscience and Neurorehabilitation, Bambino Gesù Children’s Hospital IRCCS, 00168 Rome, Italy

4. Molecular Genetics and Functional Genomics, Ospedale Pediatrico Bambino Gesù, IRCCS, 00146 Rome, Italy

Abstract

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.

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

Reference50 articles.

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3. Costello and CFC syndrome study group in Japan. Prevalence and clinical features of Costello syndrome and cardio-faciocutaneous syndrome in Japan: Findings from a nationwide epidemiological survey;Abe;Am. J. Med. Genet. A,2012

4. Adam, M.P., Mirzaa, G.M., Pagon, R.A., Wallace, S.E., Bean, L.J.H., Gripp, K.W., and Amemiya, A. (2007). GeneReviews®, University of Washington.

5. The RASopathies;Rauen;Annu. Rev. Genomics. Hum. Genet.,2013

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