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Nievergelt syndrome (mesomelic dwarfism-type Nievergelt).

作者信息

Young L W, Wood B P

出版信息

Birth Defects Orig Artic Ser. 1974;10(5):81-6.

PMID:4469999
Abstract
摘要

相似文献

1
Nievergelt syndrome (mesomelic dwarfism-type Nievergelt).
Birth Defects Orig Artic Ser. 1974;10(5):81-6.
2
Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?
Am J Med Genet. 1990 Sep;37(1):10-4. doi: 10.1002/ajmg.1320370104.
3
[Mesomelic dwarfism (author's transl)].
Rofo. 1975 Nov;123(5):450-4. doi: 10.1055/s-0029-1230234.
4
[Familial mesomelial dwarfism (Nievergelt syndrome)].
Schweiz Med Wochenschr. 1978 Aug 5;108(31):1202-6.
5
Letter re: fibula aplasia, tibial campomelia, and oligodactyly.
Am J Med Genet A. 2006 May 15;140(10):1127. doi: 10.1002/ajmg.a.31228.
6
Longitudinal tibial epiphyseal bracket in Nievergelt syndrome.
Skeletal Radiol. 1989;18(2):121-5. doi: 10.1007/BF00350660.
7
[Ulno-fibular dysplasia. An autosome-dominant hereditary micromesomelia resembling the Nievergelt syndrome].
Fortschr Geb Rontgenstr Nuklearmed. 1967 Sep;107(3):379-91.
8
Limb deficiency syndrome in half-sibs.
Clin Genet. 1981 Dec;20(6):432-7. doi: 10.1111/j.1399-0004.1981.tb01054.x.
9
Nievergelt-Pearlman syndrome with impairment of hearing. Report of three cases in a family.
J Bone Joint Surg Br. 1975 Aug;57(3):367-72.
10
Symphalangism with metacarpophalangeal fusions and elbow abnormalities.
Pediatr Radiol. 1976 Feb 13;4(2):103-7. doi: 10.1007/BF00973952.

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2
Concomitant rhomboid-shaped tibiae and fibulae, finger-like projections, and orthopedic management in a new variant of nievergelt syndrome: A case report.Nievergelt综合征新变体中的伴发菱形胫骨和腓骨、指状突起及骨科处理:一例报告
Int J Surg Case Rep. 2018;42:109-115. doi: 10.1016/j.ijscr.2017.12.002. Epub 2017 Dec 8.
3
Longitudinal tibial epiphyseal bracket in Nievergelt syndrome.
Skeletal Radiol. 1989;18(2):121-5. doi: 10.1007/BF00350660.
4
Acromesomelic dwarfism: description of a patient and comparison with previously reported cases.
Hum Genet. 1976 Sep 10;34(1):107-13. doi: 10.1007/BF00284447.