Artigo Revisado por pares

WERNER'S SYNDROME (PROGERIA OF THE ADULT) AND ROTHMUND'S SYNDROME: TWO TYPES OF CLOSELY RELATED HEREDOFAMILIAL ATROPHIC DERMATOSES WITH JUVENILE CATARACTS AND ENDOCRINE FEATURES; A CRITICAL STUDY WITH FIVE NEW CASES

1945; American College of Physicians; Volume: 23; Issue: 4 Linguagem: Inglês

10.7326/0003-4819-23-4-559

ISSN

1539-3704

Autores

S. J. Thannhauser,

Tópico(s)

RNA regulation and disease

Resumo

Article1 October 1945WERNER'S SYNDROME (PROGERIA OF THE ADULT) AND ROTHMUND'S SYNDROME: TWO TYPES OF CLOSELY RELATED HEREDOFAMILIAL ATROPHIC DERMATOSES WITH JUVENILE CATARACTS AND ENDOCRINE FEATURES; A CRITICAL STUDY WITH FIVE NEW CASESS. J. THANNHAUSERS. J. THANNHAUSERAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-23-4-559 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptObservations on these rare and apparently heredofamilial disorders are scattered throughout the different branches of medical literature according to the particular interest of the individual author specializing in involvement of the eye or the skin or the nervous system.B. S. Oppenheimer and V. S. Kugel (1934) have the distinction of first reporting this condition in American medical literature, renaming it "Werner's syndrome." The characteristics of this syndrome are:Shortness of stature, characteristic habitusCanities (i.e., premature graying of the hair)Premature baldnessScleropoikilodermaTrophic ulcers of the legsJuvenile cataractsHypogonadismTendency to diabetesCalcification of the blood vessels...Bibliography I II III1. WERNER CW: Über Katarakt in Verbindung mit Sclerodermie, Inaug. Dissert., Kiel, 1904. Google Scholar2. VOSSIUS A: Zwei Fälle von Katarakt in Verbindung mit Schlerodermie, Ztschr. f. Augenh., 1920, xliii, 640. Google Scholar3. GUILLAINALAJOUANINEMARQUEZY GTR: Sclerodermie progressive avec cataracte double précoce chez un infantile, Bull. et mém. Soc. méd. d. hôp. de Paris, 1923, xxxix, 1489. Google Scholar4. MANJUKOWA N: Zur Frage über den Zusammenhang der Linsentrübungen mit Störungen der inneren Sekretion, Ruski Ophth. Jour. 2, Klin. Monatsbl. f. Augenh., 1923, lxx, 785. Google Scholar5. PAPASTRATIYAKIS C: Un nouveau syndrome dystrophique juvenile, Paris méd., 1922, xlv, 475. 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THANNHAUSER SJ: Hereditary ectodermal dysplasia of the anhydrotic and hydrotic types, Practitioner: Library of Med. and Surg., 1938, Appleton-Century Co., New York, xiii, 473. Google Scholar This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAffiliations: *Received for publication December 26, 1944.From the Joseph H. Pratt Diagnostic Hospital and Tufts College Medical School, Boston, Mass. Aided by grants from the Rockefeller Foundation and the Godfrey Hyams Trust Fund. PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics Cited byCongenital and Childhood CataractsWerner Syndrome as a Model of Human Aging"…Rewritten in the Skin": Clues to Skin Biology and Aging from Inherited DiseaseMicrowave-Assisted Synthesis of a MK2 Inhibitor by Suzuki-Miyaura Coupling for Study in Werner Syndrome CellsLate Life Human DevelopmentPremature Ageing SyndromesUse of p38 MAPK Inhibitors for the Treatment of Werner SyndromeSarcoma Epidemiology and Etiology: Potential Environmental and Genetic FactorsCongenital and Childhood CataractsWerner Syndrome as a Model of Human AgingCorrespondenceA mouse model of Werner Syndrome: what can it tell us about aging and cancer?Hutchinson–Gilford progeria syndromeClinical Aspects of Werner's Syndrome: Its Natural History and the Genetics of the DiseaseA Report of Two Cases of Werner's Syndrome and Review of the LiteratureThe ProgeriasWhat can we learn from Werner syndrome? 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Malignant involvement of the skin and the genodermatosesGrowth hormone binding protein in Werner's syndromeGenetic linkage of Werner's syndrome to five markers on chromosome 8Werner's Syndrome: A Libyan Family with Nine Affected MembersTreatment of the Poikilodermatous Component of the Rothmund-Thomson Syndrome with the Flashlamp-Pumped Pulsed Dye Laser: A Case ReportCellular senescence: A reflection of normal growth control, differentiation, or aging?Rothmund-Thomson syndrome: a report of two patients and a review of the literatureWerner's Syndrome, Pheochromocytoma due to an Abdominal Paraganglioneuroma, and Geophagia in an ArabMetabolism of acetylated low density lipoproteins by monocyte-derived macrophages from patients with Werner's syndrome.Peripheral Vascular Reconstruction in Werner's Syndrome—A Case ReportMusculoskeletal manifestations of Werner's syndromeChanges in chromatin structure during the aging of cell cultures as revealed by differential scanning calorimetryCorneal Metastatic Calcification in Werner's SyndromeA Case of a Delusional Psychotic Syndrome in the Setting of Werner's Syndrome (Adult Progeria)2 Cases of Werner's syndrome with metabolic disturbance: Hyperlipidemia and hyperinsulinism.Bladder carcinoma with werner syndromeWerner's SyndromeWERNER'S SYNDROME (Adult Progeria)Syndromes of Premature AgingDiminished Response of Werner's Syndrome Fibroblasts to Growth Factors PDGF and FGFLymphocyte proliferation and nucleoid sedimentation in a case of premature aging distinct from Werner's syndromePortraits and BiographiesThe TestisWerner's Syndrome: A Review of its Symptomatology, Natural History, Pathologic Features, Genetics and Relationship to the Natural Aging ProcessWerner Syndrome: A Review of Recent Research with an Analysis of Connective Tissue Metabolism, Growth Control of Cultured Cells, and Chromosomal AberrationsIn Vitro Studies of Werner Syndrome Cells: Aberrant Growth and Chromosome BehaviorThe occurrence of soft tissue sarcomas in three siblings with Werner's syndromeSerum cholesterol and triglyceride levels in progeria as a model of ageingWerner's syndrome: An underdiagnosed disorder resembling premature agingGenetic and Congenital DisordersWerner's Syndrome: Twenty-four Cases with a Review of the Japanese Medical LiteratureCan We Learn about Aging from a Study of Werner's Syndrome?Werner's syndrome: A review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrationsCompendiumHyperplasias, Aplasias, Dysplasias, and AtrophiesWerner's syndromeHuman Genetic Disorders That Feature Premature Onset and Accelerated Progression of Biological AgingDermo-epidermale ErkrankungenTestisRothmund-Thomson syndrome (Poikiloderma congenitale) associated with mental retardation, growth disturbance, and skeletal featuresProgeria: Autopsy Report of One Case, with a Review of Pathologic Findings Reported in the Literature*Werner's syndrome as "Hyaluronuria"Werner's Syndrome: Autopsy Report of One Case, with a Review of Pathologic Findings Reported in the LiteratureKlinik des Diabetes mellitusThe premature ageing syndromes.The PancreasTestisWerner-Syndrom Eine hereditäre Erkrankung vieler Organsysteme*Cytoplasmic inclusion bodies within neurons of the thalamus in myotonic dystrophyAlopecia: Syndromes of Genetic SignificanceDermo-epidermale ErkrankungenWerner's syndromeCorneal Changes in Ectodermal DysplasiaThe Hutchinson-Gilford progeria syndromeTHE ROTHMUND-THOMSON SYNDROME: Case Report of an Unusual SyndromePROGERIA AND WERNER'S SYNDROME AS MODELS FOR THE STUDY OF NORMAL HUMAN AGING*The Dentition in Rothmund's SyndromePoikiloderma vasculare atrophicansSkin, heredity, and cancerThe serum growth-hormone response to hypoglycemia in dwarfismWerner's Syndrome ('Progeria of the Adult')Hereditary Disorders with Variable Malignant Neoplastic PredispositionThe General Appearance (Habitus)Werner's SyndromeTHOMAS R. RILEY, M.D., RALPH G. WIELAND, M.D., JOHN MARKIS, B.A., GEORGE J. HAMWI, M.D., F.A.C.P.Werner's SyndromeCHARLES J. EPSTEIN, M.D.Werner's Syndrome*Case 48-1963Werner's Syndrome: Progeria in the AdultDwarfism with skin manifestationsMeso-Ectodermal Dysplasia and its Variants* *From the Department of Ophthalmology, Northwestern University Medical School and the Chicago-Wesley Memorial Hospital, and the Dispensary of Presbyterian-St. Luke's Hospital and the College of Medicine, University of Illinois, and the Illinois Research Hospital.Fehlbildungen der Haut und Hautveränderungen bei FehlbildungssyndromenDie HaareRothmund-Syndrom, kombiniert mit Osteogenesis imperfecta tarda und Sarkom des OberschenkelsMale hypogonadismElastosis Perforans (Perforating Elastosis)Necrobiosis Lipoidica, Granuloma Annulare, and Rheumatoid Nodule**From the University of Pennsylvania, Departments of Dermatology, School of Medicine and Graduate School of Medicine, Philadelphia, Penna.Der Hypogonadismus im Knaben- und MannesalterA REVIEW OF WERNER'S SYNDROME, WITH A REPORT OF THE SECOND AUTOPSIED CASE*JOSEPH K. PERLOFF, M.D., ELBERT T. PHELPS, M.D., F.A.C.P.Ectodermal DysplasiaEntwicklungsstörungenEntwicklungsstörungen�ber die Formen der congenitalen PoikilodermieWERNER'S SYNDROME IN THREE SIBLINGSCasesHeritable disorders of connective tissueDie progressive SklerodermieThe Medical Significance of Lenticular Opacities (Cataract) before the Age of Fifty�ber das Rothmund-Syndrom�ber das Rothmund- und das Werner-SyndromSection of DermatologyDie progressive Sklerodermie und die dabei zu erhebenden R�ntgenbefundeWERNER'S SYNDROME.Werner's Syndrome.: A Survey Based on two CasesThe Mechanism and Incidence of Cardiovascular Changes in Paget's Disease (Osteitis Deformans)Juvenile type of werner's syndromeProgeria (Hutchinson-Gilford Syndrome): Report of a Case and Review of the LiteratureROYAL SOCIETY OF MEDICINEWerner's SyndromeCutaneous MedicineExamples of dental dysplasia 1 October 1945Volume 23, Issue 4Page: 559-626KeywordsBlood vesselsCataractsEye diseasesHypogonadismNervous systemSkin diseasesUlcers ePublished: 1 December 2008 Issue Published: 1 October 1945 PDF downloadLoading ...

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