Hereditary Ectodermal Dysplasia of the Anhidrotic Type

W Gordon, Robert C. Jamieson

Annals of Internal Medicine · 1931 · 37 citations · 10 references

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Article1 September 1931Hereditary Ectodermal Dysplasia of the Anhidrotic TypeWILLIAM H. GORDON, M.D., F.A.C.P., ROBERT C. JAMIESON, M.D.WILLIAM H. GORDON, M.D., F.A.C.P.Search for more papers by this author, ROBERT C. JAMIESON, M.D.Search for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-5-3-358 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptIn making a report of this case which we feel belongs to the group described by Goeckermann6 in 1920, MacKee and Andrews12 in 1924, Weech24 in 1929 and Jean Smith18 in 1929, it is deemed hardly necessary to review in detail the cases comprising the list that has been so ably brought up to date by the authors mentioned.We therefore will give a detailed description of this case and give tables of the chronology and clinical and pathological features to conform to those in MacKee and Andrews'12work in order to give uniformity to the reports of cases to...References1 ASCHER B: Geschwister mit Anomalien der Ohren, der Zähne und der Haut, Verhandl. d. Berl. Gesellsch. f. Anthrop., 1898, 114-121. Google Scholar2 CHRIST J: Ueber die kongenital ektodermalen Defekte und ihre Beziehungen zu einander; vikariierende Pigment für Haarbildung, Arch. f. Dermat. u. Syph., 1913, cxvi, 685-703. CrossrefGoogle Scholar3 CLOUSTON HR: Hereditary ectodermal dystrophy, Canad. Med. Assoc. Jr., 1929, xxi, 18-31. Google Scholar4 FALCONER AW: Congenital ectodermal defect, Lancet, 1929, ii, 656-658. CrossrefGoogle Scholar5 GIBBS JH: Total absence of teeth in two brothers, Dental Record, 1915, xxxv, 669-671. Google Scholar6 GOECKERMAN WH: Congenital ectodermal defect, report of case, Arch. Dermat. and Syphil., 1920, i, 396. CrossrefGoogle Scholar7 GUILFORD SH: A dental anomaly, Dental Cosmos, 1883, xxv, 113-118. Google Scholar8 GILFORD H: Progeria; a form of senilism, Practitioner, 1904, lxxiii, 188-217. Google Scholar9 HENRICHS H: Disease of ectodermal origin, Jr. Am. Med. Assoc., 1923, lxxx, 812. Google Scholar10 HUTCHINSON J: Congenital absence of hair and mammary glands with atrophic condition of skin and its appendages, Medico-Chirurgical Trans., 1886, lxix, 473-477. CrossrefGoogle Scholar11 KJAER T: A case of congenital total absence of permanent teeth, Dental Cosmos, 1907, xlix, 924-928. Google Scholar12 MACKEEANDREWS GMGC: Congenital ectodermal defect, Arch. Dermat. and Syphil., 1924, x, 673-701. CrossrefGoogle Scholar13 MACKAYDAVIDSON HAM: Congenital ectodermal defect, Brit. Jr. Dermat., 1929, xli, 1-5. Google Scholar14 OLIVERGILBERT EANC: Congenital alopecia, Arch. Dermat. and Syphil., 1926, xiii, 359-373. CrossrefGoogle Scholar15 OLIVERGILBERT EANC: Personal communication to Dr. Jamieson, 1931. Google Scholar16 PAPASTRATIGAKIS C: Dystrophic syndrome, Paris Méd., 1922, xii, 475-476. Google Scholar17 RUSHTON W: The total absence of dentition in a boy aged sixteen, Trans. Odontological Soc. Gr. Br., 1904, xxxvi, 199-204. Google Scholar18 SMITH J: Hereditary ectodermal dysplasia, Arch. Dis. Child., 1929, iv, 215-226. CrossrefGoogle Scholar19 STRANDBERG J: A contribution to question on the malformations of the ectoderm due to arrested development, Nord. Med. Ark., 1918, li, Part II, 1-12. Google Scholar20 TENDLAU B: Ueber angeborene und erworbene Atrophia cutis idiopathica, Arch. f. path. Anat., 1902, clxvii, 465-490. CrossrefGoogle Scholar21 THADANI KI: A toothless type of man, Jr. of Heredity, 1921, xii, 87-88. CrossrefGoogle Scholar22 THURNAM J: Two cases in which the skin, hair and teeth were very imperfectly developed, Medico-Chirurgical Trans., 1848, xxxi, 71-82. CrossrefGoogle Scholar23 LOEWYWECHSELMANN AW: Zur Physiologie und Pathologie des Wasserwechsels un der Wärmeregulation seitens des Hautorganes, Arch. f. path. Anat., 1911, ccvi, 79-121. CrossrefGoogle Scholar24 WEECH AA: Hereditary ectodermal dysplasia (congenital ectodermal defect); report of two cases, Am. Jr. Dis. Child., 1929, xxxvii, 766-790. CrossrefGoogle Scholar25 WHEELON H: Clinical significance of congenital absence of upper lateral incisor teeth, Endocrinology, 1925, ix, 35-60. CrossrefGoogle Scholar26 WIETING : Aus dem Gülhane Lehrkrankenhaus in Konstantinopel, Angeborener vollkommener Zahnmangel, Deutsche med. Wchnschr., 1911, xxxvii, 504. Google Scholar27 WILLIAMS CJ: (Young lady without hair and teeth), London Med. Gaz., 1848, xli, 336. Google Scholar This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAffiliations: Detroit, Mich.*Received for publication April 1, 1931. PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics Cited byHypohidrotic Ectodermal Dysplasia: Argument Against an Autosomal Recessive Form Clinically Indistinguishable from X-Linked Hypohidrotic Ectodermal Dysplasia (Christ-Siemens-Touraine Syndrome)Hypohidrotic ectodermal dysplasia in femalesVererbung von Haar- und NagelkrankheitenFehlbildungen der Haut und Hautveränderungen bei FehlbildungssyndromenHereditary ectodermal dysplasia of the anhidrotic type associated with primary hypogonadismCongenital Ectodermal DysplasiaSome skin manifestations in hypoparathyroidismHereditary ectodermal dysplasia of the anhidrotic type 1 September 1931Volume 5, Issue 3Page: 358-370KeywordsDysplasia ePublished: 1 December 2008 Issue Published: 1 September 1931 PDF downloadLoading ...

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