Callewaert Bert L, Urban Zsolt
Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium
Department of Human Genetics, University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pennsylvania
-related cutis laxa is characterized by generalized cutis laxa (ranging from generalized skin redundancy causing excessive skin folds to skin hyperextensibility without obvious skin folds) and distinctive facial features that may become more prominent with age. Other common findings are joint hyperlaxity in infancy and increasing risk of inguinal hernia at all ages. Progressive findings that may be present as early as childhood include ptosis, aortic root dilatation, and emphysema.
DIAGNOSIS/TESTING: The diagnosis of -related cutis laxa is established in a proband with suggestive findings and a heterozygous pathogenic (or likely pathogenic) variant in identified by molecular genetic testing.
There is no cure for -related cutis laxa. Experience in treating individuals with -related cutis laxa is very limited. Supportive care to improve quality of life, maximize function, and reduce complications is recommended and ideally involves multidisciplinary care by specialists in general surgery, cardiothoracic surgery, cardiology, pulmonology, urology, physical therapy, ophthalmology, and medical genetics. Monitor for known problems (e.g., inguinal hernias, joint hypermobility and pain) and new issues that may require interventions (e.g., ptosis, aortic root dilatation, emphysema, bladder diverticula). Positive pressure ventilation unless needed for life-threatening conditions; contact with people with respiratory infections; tobacco smoking; isometric exercise (which causes an increase in blood pressure); contact sports or activities that increase the risk for blunt abdominal trauma and/or joint injury or pain; sunbathing or tanning in order to preserve residual skin elasticity. Perinatal complications for mothers with -related cutis laxa or affected neonates have not been reported to date. Nonetheless, recommended evaluations for women with -related cutis laxa before conception and during pregnancy are pulmonary function testing and cardiovascular assessment (including aortic root diameter). Continued cardiac surveillance for six months post partum is also recommended. Additionally, women taking a beta-blocker should continue it during pregnancy; however, some other classes of medications, such as angiotensin receptor-blocking agents, are teratogenic and should be discontinued or changed to beta-blocking agents, given the increased risk for teratogenicity typically related to second- and third-trimester exposure.
-related cutis laxa is inherited in an autosomal dominant manner. About one third of individuals diagnosed with -related cutis laxa have an affected parent; about two thirds of affected individuals have the disorder as the result of a pathogenic variant. Each child of an individual with -related cutis laxa has a 50% chance of inheriting the pathogenic variant. Once the pathogenic variant has been identified in an affected family member, prenatal and preimplantation genetic testing are possible.
[疾病名称]相关的皮肤松弛症的特点是全身性皮肤松弛(范围从导致皮肤过度褶皱的全身性皮肤冗余到无明显皮肤褶皱的皮肤过度伸展)以及独特的面部特征,这些特征可能随着年龄增长而更加明显。其他常见表现包括婴儿期关节过度松弛以及各年龄段腹股沟疝风险增加。可能早在儿童期就出现的进行性表现包括上睑下垂、主动脉根部扩张和肺气肿。
诊断/检测:在具有提示性发现且通过分子基因检测在[相关基因]中鉴定出杂合致病性(或可能致病性)变异的先证者中确立[疾病名称]相关的皮肤松弛症的诊断。
[疾病名称]相关的皮肤松弛症无法治愈。治疗[疾病名称]相关的皮肤松弛症患者的经验非常有限。建议采取支持性护理以改善生活质量、最大化功能并减少并发症,理想情况下涉及普通外科、心胸外科、心脏病学、肺病学、泌尿学、物理治疗、眼科和医学遗传学等专科的多学科护理。监测已知问题(如腹股沟疝、关节活动过度和疼痛)以及可能需要干预的新问题(如上睑下垂、主动脉根部扩张、肺气肿、膀胱憩室)。除非是危及生命的情况,否则不进行正压通气;避免与呼吸道感染患者接触;避免吸烟;避免等长运动(会导致血压升高);避免接触性运动或增加腹部钝性创伤和/或关节损伤或疼痛风险的活动;避免日光浴或晒黑,以保持残留的皮肤弹性。迄今为止,尚未报道患有[疾病名称]相关的皮肤松弛症的母亲或受影响新生儿的围产期并发症。尽管如此,建议患有[疾病名称]相关皮肤松弛症的女性在受孕前和怀孕期间进行肺功能测试和心血管评估(包括主动脉根部直径)。产后还建议持续进行六个月的心脏监测。此外,服用β受体阻滞剂的女性在怀孕期间应继续服用;然而,其他一些药物类别,如血管紧张素受体阻滞剂,具有致畸性,鉴于通常与孕中期和孕晚期接触相关的致畸风险增加,应停药或改为β受体阻滞剂。
[疾病名称]相关的皮肤松弛症以常染色体显性方式遗传。约三分之一被诊断患有[疾病名称]相关的皮肤松弛症的个体有患病的父母;约三分之二的受影响个体因[相关基因]致病性变异而患病。患有[疾病名称]相关的皮肤松弛症的个体的每个孩子有50%的机会继承致病性变异。一旦在受影响的家庭成员中鉴定出[相关基因]致病性变异,就可以进行产前和植入前基因检测。