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名词信息
中 文 名:
新生儿宽颅缝
英 文 名:
neonatal wide cranial sutures
中文又称:
中文曾称:
名词来源:
所属专业:
新生儿科
所属类别:
疾病诊断名词
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Pubmed相关的文献
neonatal wide cranial sutures
相关文献:
Wide sutures and large fontanels in the newborn.
Tan KL.
Am J Dis Child. 1976 Apr;130(4):386-90. doi: 10.1001/archpedi.1976.02120050044007.
PMID:1266823
Yunis Varon syndrome.
Kulkarni ML, Vani HN, Nagendra K, Mahesh TK, Kumar A, Haneef S, Mohammed Z, Kulkarni PM.
Indian J Pediatr. 2006 Apr;73(4):353-5. doi: 10.1007/BF02825832.
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Hypophosphatasia in a newborn infant.
Tekinalp G, Yükselen A, Balkanci F, Coşkun T, Yurdakök M.
Turk J Pediatr. 1995 Jan-Mar;37(1):61-5.
PMID:7732610
Subtotal neonatal calvariectomy for severe craniosynostosis.
Hanson JW, Sayers MP, Knopp LM, Macdonald C, Smith DW.
J Pediatr. 1977 Aug;91(2):257-60. doi: 10.1016/s0022-3476(77)80823-8.
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A review of hedgehog signaling in cranial bone development.
Pan A, Chang L, Nguyen A, James AW.
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A monoallelic SEC23A variant E599K associated with cranio-lenticulo-sutural dysplasia.
Cisarova K, Garavelli L, Caraffi SG, Peluso F, Valeri L, Gargano G, Gavioli S, Trimarchi G, Neri A, Campos-Xavier B, Superti-Furga A.
Am J Med Genet A. 2022 Jan;188(1):319-325. doi: 10.1002/ajmg.a.62506. Epub 2021 Sep 28.
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3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (Ritscher-Schinzel syndrome).
Verloes A, Dresse MF, Jovanovic M, Dodinval P, Geubelle F.
Clin Genet. 1989 Mar;35(3):205-8. doi: 10.1111/j.1399-0004.1989.tb02929.x.
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Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature.
Tonni G, Panteghini M, Rossi A, Baldi M, Magnani C, Ferrari B, Lituania M.
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An unusually-wide human bregmatic Wormian bone: anatomy, tomographic description, and possible significance.
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Surg Radiol Anat. 2008 Nov;30(8):683-7. doi: 10.1007/s00276-008-0371-0. Epub 2008 Jun 4.
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Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?
Faria ÁC, Rabbi-Bortolini E, Rebouças MRGO, de S Thiago Pereira ALA, Frasson MGT, Atique R, Lourenço NCV, Rosenberg C, Kobayashi GS, Passos-Bueno MR, Errera FIV.
Am J Med Genet A. 2016 Feb;170A(2):403-409. doi: 10.1002/ajmg.a.37448. Epub 2015 Nov 14.
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