一个女性的法布里病:一个独特的案例强调了临床表现的变化
Arshiya Gupta1, Sumedh R Luthra1, Shivansh Luthra1
1Department of Medicine, Government Medical College Amritsar, Amritsar, IND.
Cureus
|October 30, 2024
概括
这份病例报告详细介绍了一名罕见的患有法布里病的女性患者,法布里病是一种遗传性疾病,导致全球基胺的积累. 早期诊断和治疗对于管理女性这种多系统性疾病至关重要.
科学领域:
- 遗传学和罕见疾病.
- 溶酶体储存障碍 溶酶体储存障碍
- 有关X系的继承权.
背景情况:
- 费布里病是一种罕见的X链 lysosomal储存障碍,由于α-galactosidase A 缺乏.
- 在GLA基因的突变导致全球基胺的积累,导致多系统性问题.
- 女性通常是无症状的携带者,但可以表现出广泛的症状.
研究的目的:
- 在一个32岁的女性身上呈现罕见的法布里病病例.
- 为了突出复杂的,多系统的临床表现在一个异卵性雌性.
- 强调考虑女性的法布里病的重要性,以便及时诊断和管理.
主要方法:
- 一个32岁的女性患者的病例报告.
- 临床评估包括症状,病史和实验室调查.
- 脏活检用于法布里病的组织病理学确认.
主要成果:
- 患者出现呼吸不良,发烧,疼痛,,高血压和慢性病.
- 实验室发现包括严重的贫血,脏参数升高和蛋白尿.
- 脏活检显示出具有特征的法布里病组织病理学.
结论:
- 这一案例强调了女性法布里病患者可能存在显著的多系统参与.
- 高可疑指数和全面的诊断对于识别女性的法布里病至关重要.
- 早期识别有助于针对性治疗,防止疾病进展和器官损伤.
关键词:
一个缺陷的α-galactosidase.心血管并发症的心血管并发症酶替代疗法是一种酶替代疗法.面料疾病是面料疾病.遗传突变 基因突变异构卵性雌性异构卵性雌性多系统参与 多系统参与神经系统症状 神经系统症状脏功能障碍 脏功能障碍一个x相关性疾病.更多相关视频
10:16In Vitro Enzyme Measurement to Test Pharmacological Chaperone Responsiveness in Fabry and Pompe Disease
Published on: December 20, 2017
8.0K
11:53Laparoscopic Oocyte Retrieval and Cryopreservation during Vaginoplasty for Treatment of Mayer-Rokitansky-Kuster-Hauser Syndrome
Published on: May 10, 2022
3.5K
相关概念视频
Disorders of the Female Reproductive System
332
The female reproductive system can be affected by several disorders, including Premenstrual Syndrome (PMS), Premenstrual Dysphoric Disorder (PMDD), endometriosis, and various forms of cancer. PMS and PMDD are cyclical conditions that cause physical and emotional distress, with symptoms that include edema, mood swings, and food cravings. PMDD is a more severe form of PMS characterized by increased symptom severity that peaks during the luteal phase and tends to improve or resolve shortly after...
332
Sex-linked Disorders
100.8K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
100.8K
Cystic Fibrosis: Pathogenesis
192
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
192
Infertility in Females
288
Female infertility is defined as the inability to conceive after a year of regular, unprotected intercourse and affects about 10–15% of couples worldwide. The primary cause of female infertility is ovulatory disorders, which hinder the release of eggs. These disorders can be classified as hypothalamic amenorrhea, polycystic ovarian syndrome (PCOS), premature ovarian failure, and hyperprolactinemic anovulation disorders.
Endometriosis, a condition characterized by abnormal growth of...
Endometriosis, a condition characterized by abnormal growth of...
288
Disorders of the Male Reproductive System
342
Men's health issues are increasingly recognized as significant, with several conditions posing common threats. Among these, testicular cancer is especially prevalent in younger men, particularly those aged 20 to 35 years. The disease often manifests as a painless mass in the testicles, sometimes accompanied by a sensation of heaviness or a dull ache.
Prostate disorders are another major concern. These conditions can impair urinary flow due to the prostate's location around the urethra....
Prostate disorders are another major concern. These conditions can impair urinary flow due to the prostate's location around the urethra....
342
Cystic Fibrosis: Management
143
Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
Sinus disease and chronic...
Sinus disease and chronic...
143
