نتایج جستجو برای: arthrogryposis

تعداد نتایج: 1172  

Journal: :Middle East Fertility Society Journal 2012

Journal: :Pediatric dentistry 1988
J C Ruff D E Emmanouil M J Pendzick

Arthrogryposis multiplex congenita is a congenital disorder distinguished by generalized joint immobility and skeletal muscle hypoplasia. Although the afflicted individual has normal intelligence, physical constraints often prevent independent living. This case report describes the successful fabrication and placement of a mouthstick prosthesis in a 19-

2012

Synonyms: MmD, Multi-minicore disease, Minicore myopathy, Multicore myopathy, Multiminicore myopathy, Minicore myopathy with hand involvement, antenatal onset minicore myopathy with arthrogryposis, Minicore myopathy with external ophthalmoplegia, Multicore myopathy with external ophthalmoplegia, Multiminicore disease with external opthalmoplegia, SEPN1-related congenital muscular dystrophy, rig...

Journal: :Journal of medical genetics 1988
U G Froster-Iskenius J R Waterson J G Hall

Two families are presented, each with two affected sibs, all four of whom seem to have a newly described and specific form of congenital contractures (arthrogryposis). The affected subjects have congenital torticollis, dysmorphic, asymmetrical, myopathic facial features, and progressive scoliosis. Two sibs had cleft palate. Malignant hyperthermia has occurred in two of the patients.

2017
Holger Hengel Alex Magee Muhammad Mahanjah Jean-Michel Vallat Robert Ouvrier Mohammad Abu-Rashid Jamal Mahamid Rebecca Schüle Martin Schulze Ingeborg Krägeloh-Mann Peter Bauer Stephan Züchner Rajech Sharkia Ludger Schöls

OBJECTIVE To explore the phenotypic spectrum and pathophysiology of human disease deriving from mutations in the CNTNAP1 gene. METHODS In a field study on consanguineous Palestinian families, we identified 3 patients carrying homozygous mutations in the CNTNAP1 gene using whole-exome sequencing. An unrelated Irish family was detected by screening the GENESIS database for further CNTNAP1 mutat...

Journal: :The Journal of pediatrics 1987
R Bendon P Dignan T Siddiqi

Arthrogryposis multiplex congenita may be defined as a systemic articular dysplasia characterized by articular rigidity in a many locations of congenital origin. A case was presented in which this clinical sign was diagnosed at prenatal phase and it may have many underlying causes.

2008
Yen-Chi Chou Wen-Rou Wong Tseng-tong Kuo Wei-Hsin Juan Hong-Shang Hong

We report an infant delivered at 31 weeks gestation with restrictive dermopathy, which is a rare autosomal recessive genodermatosis. The baby had thin, tightly adherent skin that causes arthrogryposis and respiratory insufficiency. Histological findings of the skin include flat dermal-epidermal junction, thinned dermis with compactly arranged collagen fibers, and hypoplastic appendage structure...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید