FAMILIAL SYRINGOMYELIA AND STATUS DYSRAPHICUS
1942; American College of Physicians; Volume: 16; Issue: 5 Linguagem: Inglês
10.7326/0003-4819-16-5-966
ISSN1539-3704
Autores Tópico(s)Assisted Reproductive Technology and Twin Pregnancy
ResumoArticle1 May 1942FAMILIAL SYRINGOMYELIA AND STATUS DYSRAPHICUSBERT E. MULVEY, M.D., F.A.C.P., LEA A. RIELY, M.D., F.A.C.P.BERT E. MULVEY, M.D., F.A.C.P.Search for more papers by this author, LEA A. RIELY, M.D., F.A.C.P.Search for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-16-5-966 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptDuring the last three years, we of the peripheral vascular department of the University Hospital have had the privilege of studying several members of a very interesting family. Various individuals of this group present signs and symptoms of impaired circulation to the extremities, disturbance of sensation in the lower limbs and feet, and a few members, similar disturbances in the hands. Slow-healing ulcers were present in the feet of some. Structural anomalies and the so-called stigmata of degeneration were present to an astonishing degree in nearly all the subjects examined. A striking familial resemblance was apparent in nearly all particulars,...Bibliography1. SCHLESINGER H: Die Syringomyelie, Monograph, 2d ed., 1902, Deuticke, Leipzig. Google Scholar2. FERRANNINI A: Nucleo nosolologico della siringomielia definito da una sua forme familiare sinora non descritta, Riforma med., 1894, ii, 735. Google Scholar3. NALBANDOFF SS: Vratch, 1899, p. 1399; Abstr., Rev. neurol., 1900, viii, 417. Google Scholar4. PREOBRAJENSKI PA: Syringomyelie hereditaire, Vratch, 1900, p. 120; Abstr., Rev. neurol., 1900, viii, 984. Google Scholar5. KRAFFT-EBING R: Cited by Schlesinger.1 Google Scholar6. VERHOOGENVANDERVELDE RP: La syringomyelie; maladie familiale, Soc. Roy. d. sci. med., Bruxelles, Ann. dela, 1894, iii, 267-300. Google Scholar7. BRUNS L: Familiäre Syringomyelie im Lumbosakralmark, Neurol. Zentralbl., 103, xxii, 599-602. 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To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAffiliations: Oklahoma City, Oklahoma*Received for publication June 21, 1939.Research problem No. 1, University of Oklahoma School of Medicine, Oklahoma City, Okla. PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics Cited byHereditary sensory and autonomic neuropathies — classification and clinical characteristicsSiringomielia: revisão da literatura e relato de casoAn hereditary sensory and autonomic neuropathy transmitted as an X-linked recessive trait.CompendiumExperimental Study of Ischemic Damage to the Cervical Spinal CordDie familiären OsteolysenA study of neural and extraneural findings in a large family with Friedreich's ataxiaDas OsteolysesyndromAnomalies of the spinal cordArachnodactyly - Status Dysraphicus - Gliosis 1 May 1942Volume 16, Issue 5Page: 966-994KeywordsSigns and symptomsUlcers ePublished: 1 December 2008 Issue Published: 1 May 1942 PDF downloadLoading ...
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