145 related articles for article (PubMed ID: 2628819)
1. Association of ectodermal dysplasia, ectrodactyly and macular dystrophy: EEM syndrome (case report).
Hayakawa M; Yanashima K; Kato K; Nakajima A; Yamauchi H
Ophthalmic Paediatr Genet; 1989 Dec; 10(4):287-92. PubMed ID: 2628819
[TBL] [Abstract][Full Text] [Related]
2. Ectrodactyly, ectodermal dysplasia, macular degeneration syndrome: a further contribution.
Yildirim MS; Ogun TC; Kamiş U
Genet Couns; 2006; 17(2):149-53. PubMed ID: 16970031
[TBL] [Abstract][Full Text] [Related]
3. EEM syndrome: report of a family and results of a ten-year follow-up.
Balarin Silva V; Simões AM; Marques-de-Faria AP
Ophthalmic Genet; 1999 Jun; 20(2):95-9. PubMed ID: 10420194
[TBL] [Abstract][Full Text] [Related]
4. Association of ectodermal dysplasia, ectrodactyly, and macular dystrophy: the EEM syndrome.
Ohdo S; Hirayama K; Terawaki T
J Med Genet; 1983 Feb; 20(1):52-7. PubMed ID: 6302256
[TBL] [Abstract][Full Text] [Related]
5. [A patient with anhidrotic ectodermal dysplasia].
Wolff AA; Hermans JB
Ned Tijdschr Geneeskd; 1981 Dec; 125(49):2015-8. PubMed ID: 7322221
[No Abstract] [Full Text] [Related]
6. Ophthalmological findings in ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome: a case report.
Matos AG; Gurgel VP; Yugar PJ; Yugar AS
Arq Bras Oftalmol; 2018; 81(5):440-442. PubMed ID: 30208149
[TBL] [Abstract][Full Text] [Related]
7. Ectodermal dysplasia, ectrodactyly and retinitis pigmentosa--a new syndrome.
Parkash H; Sidhu SS; Dhanani N; Grewal MS
J Indian Dent Assoc; 1983 Sep; 55(9):355-7. PubMed ID: 6586844
[No Abstract] [Full Text] [Related]
8. Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome).
Kjaer KW; Hansen L; Schwabe GC; Marques-de-Faria AP; Eiberg H; Mundlos S; Tommerup N; Rosenberg T
J Med Genet; 2005 Apr; 42(4):292-8. PubMed ID: 15805154
[TBL] [Abstract][Full Text] [Related]
9. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report.
Blanco-Kelly F; Rodrigues-Jacy da Silva L; Sanchez-Navarro I; Riveiro-Alvarez R; Lopez-Martinez MA; Corton M; Ayuso C
BMC Med Genet; 2017 Jan; 18(1):1. PubMed ID: 28061825
[TBL] [Abstract][Full Text] [Related]
10. [Familial congenital hypotrichosis with "uncombable hair," retinal pigmentary dystrophy, juvenile cataract and brachymetacarpia: another entity of the ectodermal dysplasia group].
Bork K; Stender E; Schmidt D; Berzas C; Rochels R
Hautarzt; 1987 Jun; 38(6):342-7. PubMed ID: 3654205
[TBL] [Abstract][Full Text] [Related]
11. Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance.
Souied E; Amalric P; Chauvet ML; Chevallier C; Le Hoang P; Munnich A; Kaplan J
Ophthalmic Genet; 1995 Mar; 16(1):11-5. PubMed ID: 7648037
[TBL] [Abstract][Full Text] [Related]
12. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome. Its association with conductive hearing loss.
Robinson GC; Wildervanck LS; Chiang TP
J Pediatr; 1973 Jan; 82(1):107-9. PubMed ID: 4681851
[No Abstract] [Full Text] [Related]
13. [Association of ectodermal dysplasia and syndactylia].
Boudghene-Stambouli O; Merad-Boudia A
Ann Dermatol Venereol; 1991; 118(2):107-10. PubMed ID: 1646587
[No Abstract] [Full Text] [Related]
14. [Familial juvenile macular dystrophy with congenital hypotrichosis capitis].
Becker M; Rohrschneider K; Tilgen W; Weber BH; Völcker HE
Ophthalmologe; 1998 Apr; 95(4):233-40. PubMed ID: 9623260
[TBL] [Abstract][Full Text] [Related]
15. Dystrophia retinae pigmentosa, fundus flavimaculatus and Stargardt's disease in one family.
van Meel GJ; Winkelman JE
Ophthalmologica; 1982; 184(1):13-20. PubMed ID: 7054737
[TBL] [Abstract][Full Text] [Related]
16. Splice site mutations in the P-cadherin gene underlie hypotrichosis with juvenile macular dystrophy.
Shimomura Y; Wajid M; Kurban M; Christiano AM
Dermatology; 2010; 220(3):208-12. PubMed ID: 20203473
[TBL] [Abstract][Full Text] [Related]
17. Anodontia with hypohidrotic ectodermal dysplasia in a young female: a case report.
Ohno K; Ohmori I
Pediatr Dent; 2000; 22(1):49-52. PubMed ID: 10730287
[TBL] [Abstract][Full Text] [Related]
18. Novel homozygous sequence variants in the CDH3 gene encoding P-cadherin underlying hypotrichosis with juvenile macular dystrophy in consanguineous families.
Ahmad F; Ali RH; Muhammad D; Nasir A; Umair M; Wakil SM; Ramzan K; Basit S; Ahmad W
Eur J Dermatol; 2016 Dec; 26(6):610-612. PubMed ID: 27456782
[No Abstract] [Full Text] [Related]
19. Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy.
Hull S; Arno G; Robson AG; Broadgate S; Plagnol V; McKibbin M; Halford S; Michaelides M; Holder GE; Moore AT; Khan KN; Webster AR
JAMA Ophthalmol; 2016 Sep; 134(9):992-1000. PubMed ID: 27386845
[TBL] [Abstract][Full Text] [Related]
20. The first reported case of
Al Zubi K; Mwafi N; Alrawashdeh HM; Al Sarireh F; Somkuwar A; Abdulmannan DM
Ophthalmic Genet; 2022 Jun; 43(3):420-424. PubMed ID: 35038959
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
