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DOI 10.1002/ajmg.a.33498

Медицинская библиотека · American journal of medical genetics. Part A · 2010

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

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

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Аннотация

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) Am J 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.

Для цитирования: Kosho Tomoki, Miyake Noriko, Hatamochi Atsushi, Takahashi Jun, Kato Hiroyuki, Miyahara Teruyoshi, Igawa Yasuhiko, Yasui Hiroshi, Ishida Tadao, Ono Kurahito, Kosuda Takashi, Inoue Akihiko, Kohyama Mohei, Hattori Tadashi, Ohashi Hirofumi, Nishimura Gen, Kawamura Rie, Wakui Keiko, Fukushima Yoshimitsu, Matsumoto Naomichi. A new Ehlers-Danlos syndrome with craniofacial characteristics, multiple congenital contractures, progressive joint and skin laxity, and multisystem fragility-related manifestations.. American journal of medical genetics. Part A. 2010. DOI: 10.1002/ajmg.a.33498.

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