Feeding and Nutritional Key Features of Crisponi/Cold-Induced Sweating Syndrome

Author:

Onesimo Roberta1ORCID,Sforza Elisabetta2ORCID,Palermo Federica2,Giorgio Valentina1ORCID,Leoni Chiara1ORCID,Rigante Donato12ORCID,Trevisan Valentina1ORCID,Agazzi Cristiana2,Limongelli Domenico1,Proli Francesco1ORCID,Kuczynska Eliza Maria1,Crisponi Laura3ORCID,Crisponi Giangiorgio4,Zampino Giuseppe12

Affiliation:

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

2. Department of Life Sciences and Public Health, Faculty of Medicine and Surgery, Catholic University of Sacred Heart, 00168 Rome, Italy

3. Institute for Genetic and Biomedical Research (IRGB), The National Research Council (CNR), Monserrato, 09042 Cagliari, Italy

4. Independent Researcher, 09042 Cagliari, Italy

Abstract

Feeding difficulties are constantly present in patients with Crisponi/cold-induced sweating syndrome type 1 (CS/CISS1). The aim of our study was to describe their prevalence and evolution from birth to adult age. We performed an observational study at the Department of Life Sciences and Public Health, Rome. Fourteen patients were included in this study (six M; mean age: 18 years; SD: 10.62 years; median age: 15 years; age range: 6–44 years); six were adults (43%). Data on oral motor abilities from birth were collected. Meal duration, presence of swallowing reflex, dysphagia symptoms, difficulty chewing, and drooling management were assessed. At birth, all patients needed enteral feeding. Introduction of solid food was postponed beyond the age of 18 months in 43% of patients. During childhood and adolescence, mealtime was characterized by increased duration (43%) accompanied by fatigue during chewing (43%), food spillage from the nasal cavities (21%), sialorrhea (86%), and poor/reduced appetite (57%). A mature rotatory chewing skill was never achieved. This report expands the phenotype description of CS/CISS1 and also improves the overall management and prevention of complications in this ultra-rare disease.

Funder

National Recovery and Resilience Plan

Publisher

MDPI AG

Reference39 articles.

1. Autosomal recessive disorder with muscle contractions resembling neonatal tetanus, characteristic face, camptodactyly, hyperthermia, and sudden death: A new syndrome?;Crisponi;Am. J. Med. Genet.,1996

2. Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1;Crisponi;Am. J. Hum. Genet.,2007

3. Adam, M.P., Feldman, J., Mirzaa, G.M., Pagon, R.A., Wallace, S.E., Bean, L.J.H., Gripp, K.W., and Amemiya, A. (2011, March 03). Cold-Induced Sweating Syndrome Including Crisponi Syndrome, Available online: https://www.ncbi.nlm.nih.gov/books/NBK52917/.

4. Crisponi/cold-induced sweating syndrome: Differential diagnosis, pathogenesis and treatment concepts;Buers;Clin. Genet.,2020

5. Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromes;Dagoneau;Am. J. Hum. Genet.,2007

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