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Ophthalmic Paediatrics and Genetics Volume 10, 1989 - Issue 4
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Original Article

Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report)

Mutsuko Hayakawa Departments of Ophthalmology, Juntendo University School of Medicine, Hongo, Bunkyo-ku, Tokyo, 113, Japan
,
Kenji Yanashima Departments of Ophthalmology, Juntendo University School of Medicine, Hongo, Bunkyo-ku, Tokyo, 113, Japan
,
Kazuo Kato Departments of Ophthalmology, Juntendo University School of Medicine, Hongo, Bunkyo-ku, Tokyo, 113, Japan
,
Akira Nakajima Departments of Ophthalmology, Juntendo University School of Medicine, Hongo, Bunkyo-ku, Tokyo, 113, Japan
&
Hiroo Yamauchi Departments of Orthopedic Surgery, Juntendo University School of Medicine, Hongo, Bunkyo-ku, Tokyo, 113, Japan
Pages 287-292 | Published online: 08 Jul 2009

Citations (10)

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Read on this site (2)

Krishna Mukkamala, Ronald C. Gentile, Judith Willner & Stephen Tsang. (2010) Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3. Ophthalmic Genetics 31:4, pages 178-182.
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Valdir Balarin Silva, Andréa Mara Simões & Antonia Paula Marques-de-Faria. (1999) EEM syndrome: report of a family and results of a ten-year follow-up. Ophthalmic Genetics 20:2, pages 95-99.
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Articles from other publishers (8)

Ricardo Leal-Rodríguez, Tania Barragán-Arévalo, Armando Pérez-Torres, David M. Giraldo-Gómez & Juan Carlos Zenteno. (2023) Clinical, genetic, and electron microscopy of hair findings in a patient with CDH3-related hypotrichosis with juvenile macular dystrophy. Clinical Dysmorphology 32:2, pages 62-64.
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Melinda Jen & Sudha Nallasamy. (2016) Ocular manifestations of genetic skin disorders. Clinics in Dermatology 34:2, pages 242-275.
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Liat Samuelov, Eli Sprecher & Ralf Paus. (2015) The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle. Cell and Tissue Research 360:3, pages 761-771.
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L. Guazzarotti, G. Tadini, G.E. Mancini, S. Giglio, C.E. Willoughby, M. Callea, I. Sani, P. Nannini, C. Mameli, A.A. Tenconi, S. Mauri, A. Bottero, A. Caimi, M. Morelli & G.V. Zuccotti. (2015) Phenotypic heterogeneity and mutational spectrum in a cohort of 45 Italian males subjects with X-linked ectodermal dysplasia. Clinical Genetics 87:4, pages 338-342.
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Bernard Puech & Jean-Jacques De Laey. 2014. Inherited Chorioretinal Dystrophies. Inherited Chorioretinal Dystrophies 335 341 .
Yehuda Senecky, Gabrielle J. Halpern, Dov Inbar, Joseph Attias & Mordechai Shohat. (2001) Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings. American Journal of Medical Genetics 101:3, pages 195-197.
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T Eke, G Woodruff & I D Young. (1996) A new oculorenal syndrome: retinal dystrophy and tubulointerstitial nephropathy in cranioectodermal dysplasia.. British Journal of Ophthalmology 80:5, pages 490-491.
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Elizabeth Bonnar, Patricia Logan & Peter Eustace. (1996) Absent meibomian glands: A marker for EEC syndrome. Eye 10:3, pages 355-361.
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