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Year Number of Results
1964 1
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2002 3
2005 1
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2011 3
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57 results

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Hypohidrotic Ectodermal Dysplasia Milia Treatment With Fractional Carbon Dioxide Laser and Laser-Assisted Drug Delivery of Triamcinolone.
Mineroff J, Dowling JR, Golbari NM, Wechter T, Jagdeo J. Mineroff J, et al. J Drugs Dermatol. 2023 Nov 1;22(11):1130-1132. doi: 10.36849/JDD.7650. J Drugs Dermatol. 2023. PMID: 37943264
Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder characterized by hypohidrosis, hypodontia, and hypotrichosis. ...The facial skin rashes caused by HED demonstrate an unmet clinical need in dermatology. Current therapies are limited to prevention …
Hypohidrotic ectodermal dysplasia (HED) is a genetic disorder characterized by hypohidrosis, hypodontia, and hypotrichosis. .. …
Ectrodactyly-Ectodermal Dysplasia-Cleft Syndrome: Ocular Findings and Surgical Treatment.
Grauhan LD, Gericke A, Brueggemann FB, Pfeiffer N, Wasielica-Poslednik J. Grauhan LD, et al. Cornea. 2023 Sep 1;42(9):1172-1175. doi: 10.1097/ICO.0000000000003295. Epub 2023 Jun 21. Cornea. 2023. PMID: 37351863
PURPOSE: Ectrodactyly-ectodermal dysplasia-cleft (EEC) syndrome is a rare genetic disorder. ...Allogeneic simple limbal epithelial transplantation (allo SLET), penetrating keratoplasty combined with allo SLET, and in total 5 amniotic membrane transplantation were pe …
PURPOSE: Ectrodactyly-ectodermal dysplasia-cleft (EEC) syndrome is a rare genetic disorder. ...Allogeneic simple limbal epithe …
Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency.
Kawai T, Nishikomori R, Heike T. Kawai T, et al. Allergol Int. 2012 Jun;61(2):207-17. doi: 10.2332/allergolint.12-RAI-0446. Allergol Int. 2012. PMID: 22635013 Free article. Review.
Anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) is characterized according to its various manifestations, which include ectodermal dysplasia, vascular anomalies, osteopetrosis, and diverse immunological abnormalities such as susceptibili …
Anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) is characterized according to its various manifestations, which …
Oral management of children/adolescents with ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome: A scoping review.
Garrocho-Rangel A, Serrano-Aguilar G, Hernández-Molinar Y, Aranda-Romo S, Alejandri-Gamboa V, Pozos-Guillén A. Garrocho-Rangel A, et al. Spec Care Dentist. 2023 Mar;43(2):152-162. doi: 10.1111/scd.12752. Epub 2022 Jul 25. Spec Care Dentist. 2023. PMID: 35879828 Review.
AIMS: EEC is a rare syndrome characterized by the triad of ectrodactyly, ectodermal dysplasia, and orofacial clefting, along with other clinical manifestations mainly in hair, skin, and teeth. ...
AIMS: EEC is a rare syndrome characterized by the triad of ectrodactyly, ectodermal dysplasia, and orofacial clefting, along w …
Ectodermal dysplasia: important role of complex dental care in its interdisciplinary management.
Kratochvilova L, Dostalova T, Schwarz M, Macek M Jr, Marek I, Malíková M, Míšová E. Kratochvilova L, et al. Eur J Paediatr Dent. 2022 Jun;23(2):140-146. doi: 10.23804/ejpd.2022.23.02.12. Eur J Paediatr Dent. 2022. PMID: 35722846 Free article.
AIM: Despite the fact that ectodermal dysplasia (ED) is a rare disease, it is often seen in a tertiary clinic. ED affects ectodermal tissues such as skin, hair, teeth, nails, and sweat glands. ...
AIM: Despite the fact that ectodermal dysplasia (ED) is a rare disease, it is often seen in a tertiary clinic. ED affects e …
A Causal Treatment for X-Linked Hypohidrotic Ectodermal Dysplasia: Long-Term Results of Short-Term Perinatal Ectodysplasin A1 Replacement.
Schneider H, Schweikl C, Faschingbauer F, Hadj-Rabia S, Schneider P. Schneider H, et al. Int J Mol Sci. 2023 Apr 12;24(8):7155. doi: 10.3390/ijms24087155. Int J Mol Sci. 2023. PMID: 37108325 Free PMC article.
X-linked hypohidrotic ectodermal dysplasia (XLHED), caused by a genetic deficiency of ectodysplasin A1 (EDA1), is a rare developmental disorder of ectodermal derivatives such as hair, sweat glands, and teeth. ...
X-linked hypohidrotic ectodermal dysplasia (XLHED), caused by a genetic deficiency of ectodysplasin A1 (EDA1), is a rare devel …
Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management.
Pinna R, Cocco F, Campus G, Conti G, Milia E, Sardella A, Cagetti MG. Pinna R, et al. Periodontol 2000. 2019 Jun;80(1):12-27. doi: 10.1111/prd.12261. Periodontol 2000. 2019. PMID: 31090139 Review.
They are inherited disorders characterized by a multisystem involvement. This review describes chondro-ectodermal dysplasia, dyskeratosis congenita, Ehlers-Danlos syndrome, hereditary benign intraepithelial dyskeratosis, keratosis follicularis, lipoid proteinosis, m …
They are inherited disorders characterized by a multisystem involvement. This review describes chondro-ectodermal dysplasia, d …
Future developments in XLHED treatment approaches.
Huttner K. Huttner K. Am J Med Genet A. 2014 Oct;164A(10):2433-6. doi: 10.1002/ajmg.a.36499. Epub 2014 Mar 26. Am J Med Genet A. 2014. PMID: 24678015 Review.
X-linked hypohidrotic ectodermal dysplasia (XLHED) is the most common genetic disorder of ectoderm development, presenting with abnormalities of skin, teeth, hair, and secretory glands. ...Survival into childhood and beyond is associated with severe dental abnormali …
X-linked hypohidrotic ectodermal dysplasia (XLHED) is the most common genetic disorder of ectoderm development, presenting wit …
Differential diagnosis portfolio of a pediatric rheumatologist: eight cases, eight stories.
Çakan M, Karadağ ŞG, Ayaz NA. Çakan M, et al. Clin Rheumatol. 2021 Feb;40(2):769-774. doi: 10.1007/s10067-020-05287-x. Epub 2020 Jul 12. Clin Rheumatol. 2021. PMID: 32656661 Review.
Definitive diagnoses of the patients were as follows: acute lymphoblastic leukemia (two cases), bilineage acute leukemia, Hodgkin lymphoma, brucellosis, mucolipidosis type III, anhidrotic ectodermal dysplasia, and Freiberg disease. In children presenting with rheuma …
Definitive diagnoses of the patients were as follows: acute lymphoblastic leukemia (two cases), bilineage acute leukemia, Hodgkin lymphoma, …
Who's your data? Primary immune deficiency differential diagnosis prediction via machine learning and data mining of the USIDNET registry.
Méndez Barrera JA, Rocha Guzmán S, Hierro Cascajares E, Garabedian EK, Fuleihan RL, Sullivan KE, Lugo Reyes SO. Méndez Barrera JA, et al. Clin Immunol. 2023 Oct;255:109759. doi: 10.1016/j.clim.2023.109759. Epub 2023 Sep 9. Clin Immunol. 2023. PMID: 37678719
RESULTS: The twelve PID diagnoses were CVID (1098 patients), DiGeorge syndrome, Chronic granulomatous disease, Congenital agammaglobulinemia, PID not otherwise classified, Specific antibody deficiency, Complement deficiency, Hyper-IgM, Leukocyte adhesion deficiency, ectodermal …
RESULTS: The twelve PID diagnoses were CVID (1098 patients), DiGeorge syndrome, Chronic granulomatous disease, Congenital agammaglobulinemia …
57 results