Zweymuller Weisenbach Syndrome

Cohen J, Currarino G, Neuhauser EBD. A significant variant in the ossification centers of the vertebral bodies. AJR Am J Roentgenol 1956; 76: 469-72 Cortina H, Vidal J, Vallcanera A, Alberto C, Muro D, Dominguez F. Humero-spinal dysostosis. Pediatr Radiol 1979; 24: 188-90 Currarino G. Unusual bone dysplasia featuring severe platyspondyly and vertebral "coronal cleft" in infancy, and changes of metaphyseal chondrodysplasia in childhood. Pediatr Radiol 1986; 16: 433-6 Epstein BS. Developmental anomalies. In: Epstein BS (ed.) The spine: a radiological text and atlas. Lea & Febiger, Philadelphia, 1976 (4th ed),pp. 185-9 Greally MT, Jewett T, Smith WL Jr, Penick GD,Williamson RA. Lethal bone dysplasia in a fetus with manifestations of atelosteogenesis I and boomerang dysplasia. Am J Med Genet 1993; 47: 1086-91 Handmaker SD, Campbell JA, Robinson LD, Chinwah O, Gorlin RJ. Dyssegmental dwarfism: a new syndrome of lethal dwarfism. Birth Defects Orig Art Ser 1977; 13: 79-90 Macpherson RI, Genez B. Spine. In: Reed MH (ed.) Pediatric skeletal radiology. Williams & Wilkins, Baltimore, 1992, pp. 231-2

Maroteaux P, Spranger J, Stanescu V, Le Marec B, Pfeiffer RA, Beighton P, Mattei JF. Atelosteogenesis. Am J Med Genet 1982; 13: 15-25

Pihlajamaa T, Prockop DJ, Faber J, Winterpacht A, Zabel B, Giedion A, Wiesbauer P, Spranger J, Ala-Kokko L. Heterozygous glycine substitution in the COL11A2 gene in the original patient with the Weissenbacher-Zweymuller syndrome demonstrates its identity with heterozygous OSMED (nonocular Stickler syndrome). Am J Med Genet 1998; 80: 115-20 Sillence D, Worthington S, Dixon J, Osborn R, Kozlowski K. Atelosteogenesis syndromes: a review, with comments on their pathogenesis. Pediatr Radiol 1997; 27: 388-96 Stern HJ, Graham JM Jr, Lachman RS, Horton W, Bernini PM, Spiegel PK, Bodurtha J, Ives EJ, Bocian M, Rimoin DL. Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digi-tal syndrome type II. Am J Med Genet 1990; 36:183-95 Tanaka T, Uhthoff HK. Significance of resegmentation in the pathogenesis of vertebral body malformation. Acta Orthop Scand 1981;52:331-8 Tanaka T, Uhthoff HK. Coronal cleft of vertebrae, a variant of normal enchondral ossification. Acta Orthop Scand 1983; 54: 389-95

Weisenbach J, Melegh B. Vertebral anomalies in Larsen's syndrome. Pediatr Radiol 1996; 26:682-3 Weissenbacher G, Zweymuller E. Gleichzeitiges Vorkommen eines Syndroms von Pierre Robin und einer fetalen Chon-drodysplasie. Monatsschr Kinderheilkd 1964; 112:315-7 Wells TR, Landing BH, Bostwick FH. Studies of vertebral coronal cleft in rhizomelic chondrodysplasia punctata. Pediatr Pathol 1992; 12: 593-600 Westvik J, Lachman RS. Coronal and sagittal clefts in skeletal dysplasias. Pediatr Radiol 1998; 28: 764-70 Wilson AR, Wastie ML, Preston BJ, Cassar-Pullicino V, Worthington BS, McKim-Thomas H. Acquired coronal cleft vertebra. Clin Radiol 1989; 40: 167-73

Wollin DG, Elliot MB. Coronal cleft vertebrae and persistent notochordal derivatives of infancy. J Can Assoc Radiol 1961; 12:78-82

Yang SS, Roskamp J, Liu CT, Frates R, Singer DB. Two lethal chondrodysplasias with giant chondrocytes. Am J Med Genet 1983; 15:615-25

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