佩罗综合征的延迟诊断:一种罕见的遗传疾病
Mirgul Bayanova1, Aigerim Abilova1, Alisa Nauryzbayeva1
1"University Medical Center" Corporate Fund, Kerey, Zhanibek Khandar Str. 5/1, Astana, Kazakhstan.
Case reports in medicine
|January 22, 2024
概括
佩罗综合征是一种罕见的遗传疾病,涉及听力损失和神经问题. 这一案例突显了HSD17B4的复合异构性,这对家庭遗传咨询至关重要.
科学领域:
- 遗传学 遗传学 是一个
- 神经学 神经学
- 内分泌学 在内分泌学.
背景情况:
- 佩罗综合征 (PRLTS) 是一种罕见的自体逆向性疾病.
- 它与多个基因中的致病变体有关,包括HSD17B4,HARS2,CLPP,LARS2,GGPS1,RMND1,TWNK,ERAL1和PRORP.
- PRLTS表现为感觉神经听力损失和潜在的神经并发症,如周围神经病变,无氧性,智力障碍.
更多相关视频
00:06In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
13.7K
08:22A Robust Polymerase Chain Reaction-based Assay for Quantifying Cytosine-guanine-guanine Trinucleotide Repeats in Fragile X Mental Retardation-1 Gene
Published on: September 16, 2019
7.9K
相关概念视频
Inborn Errors of Metabolism
160
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
160
Pleiotropy
40.5K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.5K
Genomic Imprinting and Inheritance
34.5K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
34.5K
Pedigree Analysis
84.3K
Overview
84.3K
Karyotyping
60.6K
Overview
60.6K
Lysosomal Hydrolases
3.8K
Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
3.8K
