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Brachydactyly

机译:近距离接触

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摘要

Brachydactyly ("short digits") is a general term that refers to disproportionately short fingers and toes, and forms part of the group of limb malformations characterized by bone dysostosis. The various types of isolated brachydactyly are rare, except for types A3 and D. Brachydactyly can occur either as an isolated malformation or as a part of a complex malformation syndrome. To date, many different forms of brachydactyly have been identified. Some forms also result in short stature. In isolated brachydactyly, subtle changes elsewhere may be present. Brachydactyly may also be accompanied by other hand malformations, such as syndactyly, polydactyly, reduction defects, or symphalangism.For the majority of isolated brachydactylies and some syndromic forms of brachydactyly, the causative gene defect has been identified. In isolated brachydactyly, the inheritance is mostly autosomal dominant with variable expressivity and penetrtance.Diagnosis is clinical, anthropometric and radiological. Prenatal diagnosis is usually not indicated for isolated forms of brachydactyly, but may be appropriate in syndromic forms. Molecular studies of chorionic villus samples at 11 weeks of gestation and by amniocentesis after the 14th week of gestation can provide antenatal diagnosis if the causative mutation in the family is known. The nature of genetic counseling depends both on the pattern of inheritance of the type of brachydactyly present in the family and on the presence or absence of accompanying symptoms.There is no specific management or treatment that is applicable to all forms of brachydactyly. Plastic surgery is only indicated if the brachydactyly affects hand function or for cosmetic reasons, but is typically not needed. Physical therapy and ergotherapy may ameliorate hand function. Prognosis for the brachydactylies is strongly dependent on the nature of the brachydactyly, and may vary from excellent to severely influencing hand function. If brachydactyly forms part of a syndromic entity, prognosis often depends on the nature of the associated anomalies.
机译:近距离触碰(“短指”)是一个通用术语,指的是不相称的短指和脚趾,并形成了以骨发育不良为特征的四肢畸形组的一部分。除了A3和D型以外,各种类型的近距离畸形很少见。近距离畸形既可以作为孤立的畸形也可以作为复杂畸形综合症的一部分发生。迄今为止,已经鉴定出许多不同形式的近距离接触。有些形式也会导致身材矮小。在孤立近距离中,可能在其他地方存在细微变化。近距离畸形还可能伴有其他手畸形,例如,近距畸形,多指畸形,复位缺陷或指骨畸形。对于大多数孤立近距离近距畸形和近距离畸形的某些症状形式,已经确定了致病基因缺陷。在孤立近距离生殖中,遗传主要是常染色体显性遗传,具有可变的表达和渗透性。诊断是临床的,人体测量的和放射学的。产前诊断通常不适用于近距离接触的分离形式,但可能适用于症状形式。如果已知家族中的致病突变,则在妊娠第11周和妊娠第14周后通过羊膜穿刺术对绒毛膜绒毛标本进行分子研究,可以提供产前诊断。遗传咨询的性质既取决于家族中存在的近距离生殖的类型的遗传模式,也取决于是否存在伴随症状。没有适用于所有形式近距离接触的特异性治疗或治疗。仅在近臂触觉影响手功能或出于美容原因时才指示整形手术,但通常不需要。物理疗法和人体工程疗法可能会改善手部功能。近距离触诊的预后很大程度上取决于近距离触诊的性质,并且可能会影响手功能,从优秀到严重。如果近距离形成综合征的一部分,则预后通常取决于相关异常的性质。

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