Gupta Anish A, Gotmare Swati S, Jain Megha, Pereira Treville, Khare Pooja
Department of Oral Pathology and Microbiology, Peoples Dental Academy, Bhopal, India.
Department of Oral Pathology and Microbiology, D Y Patil University School of Dentistry, Navi Mumbai, India.
J Coll Physicians Surg Pak. 2019 Apr;29(4):381-383. doi: 10.29271/jcpsp.2019.04.381.
Hereditary ectodermal dysplasia (HED) is a rare genetic disorder chiefly affecting ectodermally derived structures including hair, nails, sweat glands etc. with pathognomic manifestations such as hypotrichosis, hypohidrosis, and hypodontia. Hypohidrotic ectodermal dysplaisa, being the most frequently encountered subtype and HED, being the rare subtype. HED is primarily transmitted through X-linked recessive trait in which the gene is carried by the female and manifested in male. Although rare, this disorder may be seen affecting lot of members of the same family. We hereby report a series of four cases with common classical manifestations accompanied with spoon shaped nails, hyperpigmentation, oligodontia and hypotrichosis. The patients were treated for prosthetic rehabilitation and were asked to wear cool clothing.
遗传性外胚层发育不良(HED)是一种罕见的遗传性疾病,主要影响外胚层衍生结构,包括毛发、指甲、汗腺等,具有毛发稀少、少汗和牙发育不全等特征性表现。少汗型外胚层发育不良是最常见的亚型,而HED是罕见亚型。HED主要通过X连锁隐性遗传,基因由女性携带,在男性中表现出来。虽然罕见,但这种疾病可能在同一家族的许多成员中出现。我们在此报告一系列4例具有常见典型表现的病例,伴有匙状甲、色素沉着、牙缺失和毛发稀少。对患者进行了修复康复治疗,并要求他们穿着凉爽的衣服。