A new Ehlers-Danlos syndrome with craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility-related manifestations

  • Tomoki Kosho
  • , Noriko Miyake
  • , Atsushi Hatamochi
  • , Jun Takahashi
  • , Hiroyuki Kato
  • , Teruyoshi Miyahara
  • , Yasuhiko Igawa
  • , Hiroshi Yasui
  • , Tadao Ishida
  • , Kurahito Ono
  • , Takashi Kosuda
  • , Akihiko Inoue
  • , Mohei Kohyama
  • , Tadashi Hattori
  • , Hirofumi Ohashi
  • , Gen Nishimura
  • , Rie Kawamura
  • , Keiko Wakui
  • , Yoshimitsu Fukushima
  • , Naomichi Matsumoto

Research output: Contribution to journalArticlepeer-review

Abstract

We previously described two unrelated patients showing characteristic facial and skeletal features, overlapping with the kyphoscoliosis type Ehlers-Danlos syndrome (EDS) but without lysyl hydroxylase deficiency [Kosho et al. (2005) AmJ Med Genet Part A 138A:282-287]. After observations of them over time and encounter with four additional unrelated patients, we have concluded that they represent a new clinically recognizable type of EDS with distinct craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility-related manifestations. The patients exhibited strikingly similar features according to their age: craniofacial, large fontanelle, hypertelorism, short and downslanting palpebral fissures, blue sclerae, short nose with hypoplastic columella, low-set and rotated ears, high palate, long philtrum, thin vermilion of the upper lip, small mouth, and micro-retrognathia in infancy; slender and asymmetric face with protruding jaw from adolescence; skeletal, congenital contractures of fingers, wrists, and hips, and talipes equinovarus with anomalous insertions of flexor muscles; progressive joint laxity with recurrent dislocations; slender and/or cylindrical fingers and progressive talipes valgus and cavum or planus, with diaphyseal narrowing of phalanges, metacarpals, and metatarsals; pectus deformities; scoliosis or kyphoscoliosis with decreased physiological curvatures of thoracic spines and tall vertebrae; cutaneous, progressive hyperextensibility, bruisability, and fragility with atrophic scars; fine palmar creases in childhood to acrogeria -like prominent wrinkles in adulthood, recurrent subcutaneous infections with fistula formation; cardiovascular, cardiac valve abnormalities, recurrent large subcutaneous hematomas from childhood; gastrointestinal, constipation, diverticula perforation; respiratory, (hemo)pneumothorax; and ophthalmological, strabismus, glaucoma, refractive errors.

Original languageEnglish
Pages (from-to)1333-1346
Number of pages14
JournalAmerican Journal of Medical Genetics, Part A
Volume152
Issue number6
DOIs
Publication statusPublished - 06-2010
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

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