A New Ehlers-Danlos Syndrome With Craniofacial Characteristics, Multiple Congenital Contractures, Progressive Joint and Skin Laxity, and Multisystem Fragility-Related Manifestations

被引:67
作者
Kosho, Tomoki [1 ]
Miyake, Noriko [2 ]
Hatamochi, Atsushi [3 ]
Takahashi, Jun [4 ]
Kato, Hiroyuki [4 ]
Miyahara, Teruyoshi [5 ]
Igawa, Yasuhiko [6 ]
Yasui, Hiroshi [7 ]
Ishida, Tadao [7 ]
Ono, Kurahito [8 ]
Kosuda, Takashi [9 ]
Inoue, Akihiko [10 ]
Kohyama, Mohei [11 ]
Hattori, Tadashi [12 ]
Ohashi, Hirofumi [13 ]
Nishimura, Gen [14 ]
Kawamura, Rie [1 ]
Wakui, Keiko [1 ]
Fukushima, Yoshimitsu [1 ]
Matsumoto, Naomichi [2 ]
机构
[1] Shinshu Univ, Sch Med, Dept Med Genet, Matsumoto, Nagano 3908621, Japan
[2] Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan
[3] Dokkyo Med Univ, Sch Med, Dept Dermatol, Mibu, Tochigi, Japan
[4] Shinshu Univ, Sch Med, Dept Orthoped, Matsumoto, Nagano 3908621, Japan
[5] Shinshu Univ, Sch Med, Dept Ophthalmol, Matsumoto, Nagano 3908621, Japan
[6] Shinshu Univ, Sch Med, Dept Urol, Matsumoto, Nagano 3908621, Japan
[7] Sapporo Med Univ, Dept Internal Med 1, Sapporo, Hokkaido, Japan
[8] Tomioka Gen Hosp, Dept Orthoped, Tomioka, Japan
[9] Tomioka Gen Hosp, Dept Pediat, Tomioka, Japan
[10] Tomioka Gen Hosp, Dept Surg, Tomioka, Japan
[11] JA Hiroshima Gen Hosp, Dept Surg, Hiroshima, Japan
[12] Aichi Childrens Hlth & Med Ctr, Dept Orthoped, Oobu, Japan
[13] Saitama Childrens Med Ctr, Div Med Genet, Saitama, Japan
[14] Tokyo Metropolitan Kiyose Childrens Hosp, Dept Radiol, Kiyose, Japan
关键词
a new type Ehlers-Danlos syndrome; craniofacial characteristics; multiple congenital contractures; joint laxity; talipes deformities; kyphoscoliosis; skin laxity; multisystem fragility; recurrent subcutaneous hematomas; SYNDROME TYPE-VI; CROSS-LINKS; GENE; MUTATIONS; FORM; FIBROBLASTS; PATIENT;
D O I
10.1002/ajmg.a.33498
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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. (C) 2010 Wiley-Liss, Inc.
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页码:1333 / 1346
页数:14
相关论文
共 22 条
[1]   Deleterious mutations in the zinc-finger 469 gene cause brittle cornea syndrome [J].
Abu, Almogit ;
Frydman, Moshe ;
Marek, Dina ;
Pras, Eran ;
Nir, Uri ;
Reznik-Wolf, Haike ;
Pras, Elon .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (05) :1217-1222
[2]  
Beighton P, 1998, AM J MED GENET, V77, P31, DOI 10.1002/(SICI)1096-8628(19980428)77:1<31::AID-AJMG8>3.0.CO
[3]  
2-O
[4]  
DIETZ HC, 2009, GENEREVIEWS GENETEST
[5]   A novel missense mutation in the galactosyltransferase-I (B4GALT7) gene in a family exhibiting facioskeletal anomalies and Ehlers-Danlos syndrome resembling the progeroid type [J].
Faiyaz-Ul-Haque, M ;
Zaidi, SHE ;
Al-Mureikhi, MS ;
Kennedy, S ;
Al-Thani, G ;
Tsui, LC ;
Teebi, AS .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2004, 128A (01) :39-45
[6]   Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome -: An autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13 [J].
Giunta, Cecilia ;
Elcioglu, Nursel H. ;
Albrecht, Beate ;
Eich, Georg ;
Chambaz, Celine ;
Janecke, Andreas R. ;
Yeowell, Heather ;
Weis, MaryAnn ;
Eyre, David R. ;
Kraenzlin, Marius ;
Steinmann, Beat .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (06) :1290-1305
[7]   EXISTENCE OF MALFUNCTIONING PRO-ALPHA-2(I) COLLAGEN GENES IN A PATIENT WITH A PRO-ALPHA-2(I)-CHAIN-DEFECTIVE VARIANT OF EHLERS-DANLOS SYNDROME [J].
HATA, R ;
KURATA, S ;
SHINKAI, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 174 (02) :231-237
[8]   Ehlers-Danlos syndrome type VIB with characteristic facies, decreased curvatures of the spinal column, and joint contractures in two unrelated girls [J].
Kosho, T ;
Takahashi, J ;
Ohashi, H ;
Nishimura, G ;
Kato, H ;
Fukushima, Y .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2005, 138A (03) :282-287
[9]  
KRESSE H, 1987, AM J HUM GENET, V41, P436
[10]  
LOEYS BL, 2008, GENEREVIEWS GENETEST