...
首页> 外文期刊>Advances in Experimental Medicine and Biology >Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay syndrome.
【24h】

Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay syndrome.

机译:毛滴虫营养不良:光敏,TTD-P,TTD,Tay综合征。

获取原文
获取原文并翻译 | 示例
           

摘要

Although the term, "trichothiodystrophy" (TTD) refers to the hair anomalies in this group of patients, this is a heterogeneous, multisystem disease in which any or every organ in the body may be affected. Neuroectodermal derived tissues are particularly likely to be involved. This term was introduced by Price et alin 1980 to designate patients with sulfur-deficient brittle hair, which they recognized as a marker for this complex disease and designated it as a neuroectodermal symptom complex (associated with reduced content ofcysteine-rich matrix proteins), ichthyotic skin and physical and mental growth retardation. Ichthyosis is usually apparent at birth but much less so after the first few weeks of life. Other frequently associated features include ocular cataracts, infections and maternal complications related to pregnancy. Atrophy of subcutaneous fat may also be present. TTD occurs in a pattern of inheritance consistent with an autosomal recessive condition. The disease is extremely heterogeneous in severity and extent, with some patients showing no neurological deficiency. Others show severe, multisystem disease. Many patients die at a young age, most commonly due to infectious disease. TTD is part of a more broadly defined group of diseases identified as IBIDS (ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature). Photosensitive cases are also identified as PIBIDS (photosensitivity with IBIDS). Cases without manifest ichthyosis are also identified as PBIDS. These syndromes defy rigorous definition because of clinical variation between patients. The original two cases were described by Tay in oriental siblings, whose parents were first cousins; thus the disease is also known as Tay syndrome. The hairs in patients with TTD have a distinctive, diagnostically useful appearance on polarized light microscopy consisting of alternating light and dark bands known as the "tiger tail" anomaly. Diagnosis may be confirmed by sulfur content analysis ofhair shafts, which shows decreased sulfur and cysteine content. Approximately half of patients with TTD have photosensitivity, which correlates with a nudeotide excision repair (NER) defect. These patients are designated as having trichothiodystrophy-photosensitive (TTDP). Non-photosensitivepatients are designated as having trichothiodystrophy-nonphotosensitive (TTDN). Skin cancer is very rare in sun-sensitive TTD.
机译:尽管术语“毛滴虫性营养不良”(TTD)指的是这类患者中的毛发异常,但这是一种异质的多系统疾病,可能会影响身体的任何器官或每个器官。神经外胚层衍生的组织特别可能涉及。 Price这个术语是由Price等人在1980年提出的,用于指定硫缺乏型脆性头发的患者,他们将其识别为这种复杂疾病的标志物,并将其命名为神经外胚层症状复合物(与富含半胱氨酸的基质蛋白含量降低有关),鱼鳞病皮肤和身心发育迟缓。鱼鳞病通常在出生时就很明显,但在生命的最初几周后就不那么明显了。其他常见的特征包括眼白内障,感染和与妊娠有关的母亲并发症。皮下脂肪也可能萎缩。 TTD以与常染色体隐性遗传状况一致的遗传模式发生。该疾病的严重程度和程度极不相同,有些患者没有神经系统疾病。其他人则表现出严重的多系统疾病。许多患者在年轻时死亡,最常见的原因是传染病。 TTD是被定义为IBIDS(鱼鳞病,头发脆弱,智力受损,生育力下降和身材矮小)的一组更广泛定义的疾病的一部分。光敏病例也被识别为PIBIDS(IBIDS的光敏性)。没有明显鱼鳞病的病例也被鉴定为PBIDS。由于患者之间的临床差异,这些综合征无法严格定义。 Tay在东方兄弟姐妹中描述了最初的两个案例,他们的父母是表亲。因此,这种疾病也称为Tay综合征。在偏光显微镜下,患有TTD的患者的头发具有独特的,对诊断有用的外观,由交替出现的亮带和暗带组成,被称为“虎尾”异常。诊断可以通过发干中的硫含量分析来证实,硫含量和半胱氨酸含量降低。大约一半的TTD患者具有光敏性,这与核苷切除修复(NER)缺陷相关。这些患者被指定为对毛发硫代营养不良症敏感(TTDP)。非光敏患者被指定为对非硫代毛发营养不良症(TTDN)。皮肤癌在对太阳敏感的TTD中非常罕见。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号