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89 Possible Causes for masuno

  • Hemivertebra

    Imaizumi K, Masuno M, Ishii T, Kuroki Y, Okuzumi N, Nakamura Y: Congenital scoliosis (hemivertebra) associated with de novo balanced reciprocal translocation, 46,XX,t(13;[karger.com]

  • Renal Coloboma Syndrome

    […] identical PAX2 mutations Authors: Schimmenti, L A Cunliffe, H E McNoe, L A Ward, T A French, M C Shim, H H Zhang, Y H Proesmans, Willem Leys, A Byerly, K A Braddock, S R Masuno[lirias.kuleuven.be]

  • Young Simpson Syndrome

    Young Simpson syndrome at NIH 's Office of Rare Diseases Kondoh T, Kinoshita E, Moriuchi H, Niikawa N, Matsumoto T, Masuno M (January 2000).[en.wikipedia.org] Masuno M, Imaizumi K, Okada T, Adachi M, Nishimura G, Ishii T, Tachibana K, Kuroki Y.[ghr.nlm.nih.gov] 1) Masuno M, Imaizumi K, Okada T, Adachi M, Nishimura G, Ishii T, Tachibana K, Kuroki Y.[kcmc.jp]

  • Frontometaphyseal Dysplasia

    Takahashi K, Kuwahara T, Tanigawara T, Hattori T, Masuno M, Kondo N: Frontometaphyseal dysplasia: patient with ruptured aneurysm of the aortic sinus of Valsalva and cerebral[koreascience.or.kr]

  • Smith-Magenis Syndrome

    Masuno M, Asano J, Arai M, Kuwahara T, Orii T (1992): Interstitial deletion of 17p11.2 with brain abnormalities. Clin Genet 41:278-280.[priory.com] ., 1991; Masuno et al., 1992; Finucane et al., 1993ab, 1994; Fischer et al., 1993; Meinecke, 1993; Zori et al., 1993; Fan and Farrell, 1994; Barmcoat et al., 1996; Greenberg[priory.com]

  • Microcephalic Osteodysplastic Primordial Dwarfism Type II

    They extend from marked metaphysealflare in the patients of Brizard et al. [1973] to someminor changes as in the patients of Masuno et al.[1995].Consanguinity in 5 out of[myslide.es] Am J Med Genet 44:203209.Masuno M, Imaizumi K, Nishimura G, Kurosawa K, Makita Y, ShimazakiY, Kuroki Y (1995): Osteodysplastic primordial dwarfism: A case withfeatures of[myslide.es] However,there was no metaphyseal widening in the patients re-ported by Halder et al. [1998] and Masuno et al. [1995].Typically in MOPD II, coxa vara deformity andepiphyseolysis[myslide.es]

  • Encephalopathy

    Tyndall , Stefania Mondello , Yasushi Shibata , Naoki Tominaga , Takahiro Kanaya , Toru Takiguchi , Yutaka Igarashi , Jun Hagiwara , Ryuta Nakae , Hidetaka Onda , Tomohiko Masuno[nature.com]

  • Endocardial Fibroelastosis

    Ohta H, Masuno M, Kimura J et al (1999) Toriello-Carey syndrome with endocardial fibroelastosis. Am J Med Genet 87:271–272 PubMed CrossRef Google Scholar 11.[link.springer.com]

  • Monosomy 1p36 Syndrome

    J Med Genet 32:619â “622 Kurosawa K, Kawame H, Okamoto N, Ochiai Y, Akatsuka A, Kobayashi M, Shimohira M, Mizuno S, Wada K, Fukushima Y, Kawawaki H, Yamamoto T, Masuno M,[ijsciences.com]

  • Young Syndrome

    Masuno M, Imaizumi K, Okada T, Adachi M, Nishimura G, Ishii T, Tachibana K, Kuroki Y.[ghr.nlm.nih.gov]

Further symptoms