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Mowat-Wilson syndrome: growth charts.


ABSTRACT:

Background

Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or deletions of the ZEB2 gene. It is characterized by moderate-severe intellectual disability, epilepsy, Hirschsprung disease and multiple organ malformations of which congenital heart defects and urogenital anomalies are the most frequent ones. To date, a clear description of the physical development of MWS patients does not exist. The aim of this study is to provide up-to-date growth charts specific for infants and children with MWS. Charts for males and females aged from 0 to 16?years were generated using a total of 2865 measurements from 99 MWS patients of different ancestries. All data were collected through extensive collaborations with the Italian MWS association (AIMW) and the MWS Foundation. The GAMLSS package for the R statistical computing software was used to model the growth charts. Height, weight, body mass index (BMI) and head circumference were compared to those from standard international growth charts for healthy children.

Results

In newborns, weight and length were distributed as in the general population, while head circumference was slightly smaller, with an average below the 30th centile. Up to the age of 7?years, weight and height distribution was shifted to slightly lower values than in the general population; after that, the difference increased further, with 50% of the affected children below the 5th centile of the general population. BMI distribution was similar to that of non-affected children until the age of 7?years, at which point values in MWS children increased with a less steep slope, particularly in males. Microcephaly was sometimes present at birth, but in most cases it developed gradually during infancy; many children had a small head circumference, between the 3rd and the 10th centile, rather than being truly microcephalic (at least 2 SD below the mean). Most patients were of slender build.

Conclusions

These charts contribute to the understanding of the natural history of MWS and should assist pediatricians and other caregivers in providing optimal care to MWS individuals who show problems related to physical growth. This is the first study on growth in patients with MWS.

SUBMITTER: Ivanovski I 

PROVIDER: S-EPMC7294656 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature

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Mowat-Wilson syndrome: growth charts.

Ivanovski Ivan I   Djuric Olivera O   Broccoli Serena S   Caraffi Stefano Giuseppe SG   Accorsi Patrizia P   Adam Margaret P MP   Avela Kristina K   Badura-Stronka Magdalena M   Bayat Allan A   Clayton-Smith Jill J   Cocco Isabella I   Cordelli Duccio Maria DM   Cuturilo Goran G   Di Pisa Veronica V   Dupont Garcia Juliette J   Gastaldi Roberto R   Giordano Lucio L   Guala Andrea A   Hoei-Hansen Christina C   Inaba Mie M   Iodice Alessandro A   Nielsen Jens Erik Klint JEK   Kuburovic Vladimir V   Lazalde-Medina Brissia B   Malbora Baris B   Mizuno Seiji S   Moldovan Oana O   Møller Rikke S RS   Muschke Petra P   Otelli Valeria V   Pantaleoni Chiara C   Piscopo Carmelo C   Poch-Olive Maria Luisa ML   Prpic Igor I   Marín Reina Purificación P   Raviglione Federico F   Ricci Emilia E   Scarano Emanuela E   Simonte Graziella G   Smigiel Robert R   Tanteles George G   Tarani Luigi L   Trimouille Aurelien A   Valera Elvis Terci ET   Schrier Vergano Samantha S   Writzl Karin K   Callewaert Bert B   Savasta Salvatore S   Street Maria Elisabeth ME   Iughetti Lorenzo L   Bernasconi Sergio S   Giorgi Rossi Paolo P   Garavelli Livia L  

Orphanet journal of rare diseases 20200615 1


<h4>Background</h4>Mowat-Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or deletions of the ZEB2 gene. It is characterized by moderate-severe intellectual disability, epilepsy, Hirschsprung disease and multiple organ malformations of which congenital heart defects and urogenital anomalies are the most frequent ones. To date, a clear description of the physical development of MWS patients does not exist. The aim of this study is to provide up-to-date g  ...[more]

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