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Caroline crachami and the delineation of osteodysplastic primordial dwarfism type III, an autosomal recessive syndrome

1992; Wiley; Volume: 44; Issue: 2 Linguagem: Inglês

10.1002/ajmg.1320440217

1096-8628

F. Majewski,

Connective tissue disorders research

American Journal of Medical GeneticsVolume 44, Issue 2 p. 203-209 Invited Editorial Comment Caroline crachami and the delineation of osteodysplastic primordial dwarfism type III, an autosomal recessive syndrome Prof. Dr. F. Majewski, Corresponding Author Prof. Dr. F. Majewski Institute of Human Genetics, University of Düsseldorf, GermanyInstitut für Humangenetik, Morrenstr. 5, 4000 Düsseldorf 1, GermanySearch for more papers by this author Prof. Dr. F. Majewski, Corresponding Author Prof. Dr. F. Majewski Institute of Human Genetics, University of Düsseldorf, GermanyInstitut für Humangenetik, Morrenstr. 5, 4000 Düsseldorf 1, GermanySearch for more papers by this author First published: 15 September 1992 https://doi.org/10.1002/ajmg.1320440217Citations: 23AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL References Bondeson J (1992) Caroline Crachami, the Sicilian fairy: A case of bird-headed dwarfism. Am J Med Genet (this issue). Boscherini B, Iannacone G, La Cauza C, Mancuso G, Girotti F, Finocchi G, Pasquino AM (1981): Intrauterine growth retardation. A report of two cases with birth-headed appearance, skeletal changes and peripheral GH resistance. Eur J Pediatr 137: 237– 242. Gilford H (1902): Ateleiosis, a disease characterized by conspicuous delay of growth and development. Med Chir Trans 85: 305– 359. Home E (1825): The Croonian lecture. On the existence of nerves in the placenta. Phil Trans R Soc London 115: 66– 80. Majewski F, Goecke T (1982): Studies of microcephalic primordial dwarfism I: Approach to a delineation of the Seckel syndrome. Am J Med Genet 12: 7– 21. Majewski F, Stoeckenius M, Kemperdick H (1982): Studies of microcephalic primordial dwarfism III: An intrauterine dwarf with platy-spondyly and anomalies of pelvis and clavicles—osteodysplastic primordial dwarfism type III. Am J Med Genet 12: 37– 42. Meinecke P, Passarge E (1991): Microcephalic osteodysplastic primordial dwarfism type I/III in sibs. J Med Genet 28: 795– 800. Meinecke P, Schaefer E, Wiedemann HR (1991): Microcephalic osteodysplastic primordial dwarfism: Further evidence for identity of the so-called types I and II. Am J Med Genet 39: 232– 236. Neumann H, Karte H (1982/83): Extremer intrauteriner mik-rozephaler Minderwuchs mit Risenaneursyma des Circulus arteriosus Willisi. Pädiat Prax 27: 21– 31. Rischbieth H, Barrington A (1912): “ Treasury of Human Inheritance,” VII, XVa. London: Cambridge Univ Press, pp 355– 553. Seckel HPG (1960): “ Bird-Headed Dwarfs.” Basel, New York: Karger. Toudic L, Roche J, Alix D, le Bars CH, Dantoine G, Castel Y (1977): Nanisme intra-utérin majeur avec dysmorphies et encéphalopathie profonde de type nanisme a téte d'oiseau (Virchow-Seckel). Ann Pediatr 24: 653– 656. Virchow R (1892): Vorstellung des Knaben Dobos Janos. Berl Klin Wschr 29: 517. Citing Literature Volume44, Issue215 September 1992Pages 203-209 ReferencesRelatedInformation