Cited by 17Lysosomal Storage Disorders ResearchConnective tissue disorders researchGenomics and Rare Diseases

Excessively redundant umbilical skin as a potential early clinical feature of Morquio syndrome and FKBP14‐related Ehlers–Danlos syndrome

Aldeeri, A.A., Alazami, A.M., Hijazi, H., Alzahrani, F., Alkuraya, F.S.·2014·Clinical Genetics

Abstract

Several umbilical abnormalities have been linked to and utilized to aid in the clinical diagnosis of certain syndromes. For instance, umbilical skin redundancy has long been recognized as a core feature of Rieger syndrome although its association with other disorders is unknown. In this article, we report for the first time the occurrence of this distinct clinical sign in association with two other syndromes: Morquio syndrome and FKBP14‐related Ehlers–Danlos syndrome (EDS). Our observation is clinically significant because patients with Morquio syndrome are often diagnosed only after they develop typical skeletal manifestations, which reduces the efficacy of available enzyme replacement therapy, so the umbilical sign we report here can facilitate a much earlier diagnosis. In addition, the extreme rarity of FKBP14‐related Ehlers–Danlos syndrome (EDS) can greatly delay the diagnosis of this condition unless it is recognized in the differential diagnosis of redundant umbilical skin as we argue in this report.

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Crossref · 10.1111/cge.12414

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  • Four different FKBP14 mutations have been identified to date.

    “Four different FKBP14 mutations have been identified to date [Baumann et al., 2012;Aldeeri et al., 2014;Murray et al., 2014;Dordoni et al., 2016].”

    From The Ehlers–Danlos syndromes, rare types (2017) · cites this paper as Aldeeri et al., 2014

  • To date, 10 patients with kEDS-FKBP14 from nine independent families have been described.

    “To date, 10 patients with kEDS-FKBP14 from nine independent families have been described: Five pediatric (<12 years), three adolescents (16 years), and two adults (42-and 48-year-old) (Table S1) [Baumann et al., 2012, Aldeeri et al., 2014, Murray et al., 2014, Alazami et al., 2016, Dordoni et al., 2016].”

    From The Ehlers–Danlos syndromes, rare types (2017) · cites this paper as Aldeeri et al., 2014

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Authors
Aldeeri, A. A., Alazami, A. M., Hijazi, H., Alzahrani, F., & Alkuraya, F. S.
Affiliations
  • King Faisal Specialist Hospital & Research Centre (SA)
  • Alfaisal University (SA)
Corresponding author
Alkuraya, F.S.
Venue
Clinical Genetics
Publisher
Wiley
Published
2014-05-22
Volume
86
Issue
5
Pages
469-472
ISSN
  • 0009-9163 (ISSN-L)
  • 1399-0004
OpenAlex
W1506360056
Cited by
17
References
1
Citations by year
2025: 1 · 2024: 1 · 2023: 1 · 2022: 1 · 2020: 2 · 2018: 1 · 2017: 4 · 2016: 4 · 2015: 2
FWCI
2.22
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Genetics (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
Keywords
Morquio syndrome, Ehlers-Danlos syndrome, early diagnosis, Rieger syndrome, differential diagnosis, enzyme replacement therapy
MeSH terms
Child, Child, Preschool, Ehlers-Danlos Syndrome, Female, Humans, Infant, Infant, Newborn, Male, Mucopolysaccharidosis IV, Skin Abnormalities, Umbilicus, Peptidylprolyl Isomerase

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