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A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report

BACKGROUND: Ehlers-Danlos syndrome (EDS) represents a group of connective tissue disorders characterized by the fragility of the soft connective tissues resulting in widespread skin, ligament, joint, blood vessel and internal organ involvement. The clinical spectrum is highly variable in terms of cl...

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Autores principales: Conti, Rosaura, Zanchi, Chiara, Barbi, Egidio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881555/
https://www.ncbi.nlm.nih.gov/pubmed/33579342
http://dx.doi.org/10.1186/s13052-021-00984-y
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author Conti, Rosaura
Zanchi, Chiara
Barbi, Egidio
author_facet Conti, Rosaura
Zanchi, Chiara
Barbi, Egidio
author_sort Conti, Rosaura
collection PubMed
description BACKGROUND: Ehlers-Danlos syndrome (EDS) represents a group of connective tissue disorders characterized by the fragility of the soft connective tissues resulting in widespread skin, ligament, joint, blood vessel and internal organ involvement. The clinical spectrum is highly variable in terms of clinical features, complications, severity, biochemical characteristics and genes mutations. The kyphoscoliotic type EDS (EDS VIA) is a rare variant of the disease, with an incidence of 1:100.000 live births. EDS VIA presents at birth as severe muscular hypotonia, early onset of progressive kyphoscoliosis, marked hyperelasticity and fragility of the skin with abnormal scarring, severe joint hypermobility, luxations and osteopenia without a tendency to fractures. This condition is due to a mutation in the PLOD1 gene, and less commonly in FKBP14 gene, which results in the erroneous development of collagen molecules with consequent mechanical instability of the affected tissue. CASE PRESENTATION: A female newborn, found to be floppy at birth, presented a remarkable physical examination for joint hypermobility, muscle weakness, hyperelastic skin, a slight curve of the spine, the absence of the inferior labial and lingual frenulum. Due to severe hypotonia, neuromuscular disorders such as Spinal Muscular Atrophy (SMA), genetic diseases such as Prader Willi syndrome (PWS), myopathies and connective tissue disorders were considered in the differential diagnosis. Targeted gene sequencing were performed for SMN1, PLOD1, FKBP14, COL6A1, COL6A2, COL6A3. The urinary lysyl and hydroxy-lysyl pyridinoline ratio was diagnostic before discovering the homozygous duplication in the PLOD1 gene, which confirmed kyphoscoliotic EDS diagnosis. CONCLUSION: In front of a floppy infant, a large variety of disorders should be considered, including some connective diseases. The presence at the birth of kyphoscoliosis, associated with joint hypermobility and the absence of the lingual and lower lip frenulum, should suggest an EDS.
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spelling pubmed-78815552021-02-17 A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report Conti, Rosaura Zanchi, Chiara Barbi, Egidio Ital J Pediatr Case Report BACKGROUND: Ehlers-Danlos syndrome (EDS) represents a group of connective tissue disorders characterized by the fragility of the soft connective tissues resulting in widespread skin, ligament, joint, blood vessel and internal organ involvement. The clinical spectrum is highly variable in terms of clinical features, complications, severity, biochemical characteristics and genes mutations. The kyphoscoliotic type EDS (EDS VIA) is a rare variant of the disease, with an incidence of 1:100.000 live births. EDS VIA presents at birth as severe muscular hypotonia, early onset of progressive kyphoscoliosis, marked hyperelasticity and fragility of the skin with abnormal scarring, severe joint hypermobility, luxations and osteopenia without a tendency to fractures. This condition is due to a mutation in the PLOD1 gene, and less commonly in FKBP14 gene, which results in the erroneous development of collagen molecules with consequent mechanical instability of the affected tissue. CASE PRESENTATION: A female newborn, found to be floppy at birth, presented a remarkable physical examination for joint hypermobility, muscle weakness, hyperelastic skin, a slight curve of the spine, the absence of the inferior labial and lingual frenulum. Due to severe hypotonia, neuromuscular disorders such as Spinal Muscular Atrophy (SMA), genetic diseases such as Prader Willi syndrome (PWS), myopathies and connective tissue disorders were considered in the differential diagnosis. Targeted gene sequencing were performed for SMN1, PLOD1, FKBP14, COL6A1, COL6A2, COL6A3. The urinary lysyl and hydroxy-lysyl pyridinoline ratio was diagnostic before discovering the homozygous duplication in the PLOD1 gene, which confirmed kyphoscoliotic EDS diagnosis. CONCLUSION: In front of a floppy infant, a large variety of disorders should be considered, including some connective diseases. The presence at the birth of kyphoscoliosis, associated with joint hypermobility and the absence of the lingual and lower lip frenulum, should suggest an EDS. BioMed Central 2021-02-12 /pmc/articles/PMC7881555/ /pubmed/33579342 http://dx.doi.org/10.1186/s13052-021-00984-y Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Case Report
Conti, Rosaura
Zanchi, Chiara
Barbi, Egidio
A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
title A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
title_full A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
title_fullStr A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
title_full_unstemmed A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
title_short A floppy infant without lingual frenulum and kyphoscoliosis: Ehlers Danlos syndrome case report
title_sort floppy infant without lingual frenulum and kyphoscoliosis: ehlers danlos syndrome case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881555/
https://www.ncbi.nlm.nih.gov/pubmed/33579342
http://dx.doi.org/10.1186/s13052-021-00984-y
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