Portal de Periódicos da CAPES

Melnick-Needles Syndrome

1978; Slack Incorporated (United States); Volume: 15; Issue: 4 Linguagem: Inglês

10.3928/0191-3913-19780701-09

1938-2405

L Douglas Perry, William C. Edwards, Robert T Bramson,

Genetic Syndromes and Imprinting

Melnick-Needles Syndrome L Douglas Perry, MD, , , MD William C Edwards, MD, , and , MD Robert T Bramson, MD, , MD L Douglas Perry, MD , William C Edwards, MD , and Robert T Bramson, MD Journal of Pediatric Ophthalmology & Strabismus, 2013;15(4):226–230Published Online:July 01, 1978https://doi.org/10.3928/0191-3913-19780701-09Cited by:7PDFView Full Text ToolsAdd to favoritesDownload CitationsTrack Citations ShareShare onFacebookTwitterLinkedInRedditEmail SectionsMore1. Melnick JC, Needles CF: An undiagnosed bone dysplasia: a 2 family study of 4 generations and 3 generations. Am J Roentgenol 97:39-48, 1966. Google Scholar2. Kaufmann HJ: Osteodysplasia (MelnickNeedles). Semin Roentgenol 8:182-183, 1973. Google Scholar3. Coste F, Maroteaux ?, Chouraki L: Osteodysplasty (Melnick and Needles syndrome): report of a case. Ann Rheum Dis 27:360-366, 1968. Google Scholar4. Leiber ?, Hovels O: Das neue syndrom: MelnickNeedles-syndrom. Monatsschr Kinderheilkd 123:178-182, 1975. Google Scholar5. Wendler VH, Kellerer K: Osteodysplasiesyndrome (Melnick-Needles). Fortschr Rontgenstr 122:309-313, 1975. Google Scholar6. Moadel E, Bryk D: Radiological quiz. Radiology 123:154,206. 1977. Google Scholar7. Shuler SE: Pycnodysostosis. Arch Dis Child 38:620-625, 1963. Google Scholar8. Lennon EA, Schechter MM, Hornabrook RW: Engelmann's disease: report of a case with a review of the literature. J Bone Joint Surg [Br] 43:273-284, 1961. Google Scholar9. Girdany BR: Engelmann's disease (progressive diaphyseal dysplasia): a nonprogressive famU'tal form of muscular dystrophy with characteristic bone changes. Clin Orthop 14:102-109, 1959. Google Scholar1 0. Krohel GB, Wirth CR: Engelmann's disease. Am J Ophthalmol 84:520-525, 1977. Google Scholar1 1 . Pyle E; A case of unusual bone development. J Bone Joint Surg 13:874-876, 1931. Google Scholar12. Keats TE, Alavi MS: Toxopachyosteose diaphysaire tibioperoniere (Weismann-Netter syndrome). Am J Roentgenol 109:568-574, 1970. Google Scholar13. Shorb SR: Bilateral ametropic amblyopia resulting from bilateral cornea plana. Am J Ophthalmol 73:663-664, 1972. Google Scholar14. Eriksson AW, Lehmann W, Forsius H: Congenital cornea plana in Finland. Clin Genet 4:301-310, 1973. Google Scholar15. Goldstein JE, Cogan DG: Sclerocornea and associated congenital anomalies. Arch Ophthalmol 67:761-768, 1962. Google Scholar16. Kolbert GS, Seelenfreund M: Sclerocornea, anterior cleavage syndrome, and trisomy Ì8. Ann Ophthalmol 2:26, 28, 30, 1970. Google Scholar17. Rodrigues MM, Calhoun J, Weinreb S: Sclerocornea with an unbalanced translocation (I7p, 10q). Am J Ophthalmol 78:49-53, 1974. Google Scholar1 8. Friedman AH, Weingeist S, Brackup A, Marinoff G: Sclero-cornea and defective mesodermal migration. Br J Ophthalmol 59:683-687, 1975. Google Scholar19. March WF, Chalkley THF: Sclerocornea associated with Dandy- Walker cyst. Am J Ophthalmol 78:54-57, 1 974. Google Scholar20. Howard RO, Abrahams IW: Sclerocornea. Am J Ophthalmol 71:1254-1260, 1971. Google Scholar Previous article Next article FiguresReferencesRelatedDetailsCited by Chang T, Bauer M, Puerta H, Greenberg M and Cavuoto K (2017) Ophthalmic findings in Frank-ter Haar syndrome: report of a sibling pair, Journal of American Association for Pediatric Ophthalmology and Strabismus, 10.1016/j.jaapos.2017.07.216, 21:6, (514-516), Online publication date: 1-Dec-2017. Murphy-Ryan M, Babovic-Vuksanovic D and Lindor N (2011) Bifid tongue, corneal clouding, and Dandy-Walker malformation in a male infant with otopalatodigital syndrome type 2, American Journal of Medical Genetics Part A, 10.1002/ajmg.a.33901, 155:4, (855-859), Online publication date: 1-Apr-2011. Gupta P and Kim T (2011) Developmental Corneal Anomalies of Size and Shape Cornea, 10.1016/B978-0-323-06387-6.00064-7, (643-653), . Moriarty A and Kerr-Muir M (1992) Sclerocornea and Interstitial Deletion of the Short Arm of Chromosome 6-(46XY del[6] [p22 p24]), Journal of Pediatric Ophthalmology & Strabismus, 10.3928/0191-3913-19920501-12, 29:3, (177-179), Online publication date: 1-May-1992. Winter R and Baraitser M (1991) A catalogue of multiple congenital anomaly syndromes Multiple Congenital Anomalies, 10.1007/978-1-4899-3109-2_1, (1-672), . Garrett C, Berry A, Simpson R and Hall C (1990) Yunis-Varon syndrome with severe osteodysplasty., Journal of Medical Genetics, 10.1136/jmg.27.2.114, 27:2, (114-121), Online publication date: 1-Feb-1990. Kivlin J, Fineman R, Williams M, Opitz J and Reynolds J (1985) Phenotypic variation in the del(12p) syndrome, American Journal of Medical Genetics, 10.1002/ajmg.1320220412, 22:4, (769-779), Online publication date: 1-Dec-1985. Request Permissions InformationCopyright 2013, SLACK IncorporatedPDF download