CATSHL综合征,一个新的家族和表型扩展
Silvia Cannova1, Camilla Meossi2, Federico Grilli2
1Università degli Studi di Milano, Milano, Italy.
Clinical genetics
|November 22, 2023
概括
一种新的FGFR3基因变异导致CATSHL综合征,这种疾病的特点是身高高大,骨异常和听力损失. 这一发现扩大了我们对CATSHL和相关疾病的遗传基础的理解.
科学领域:
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
- 医学遗传学 医学遗传学
背景情况:
- 纤维细胞生长因子受体3 (FGFR3) 突变与各种骨功能失调有关.
- 坎普托达克提 - 高身高 - 脊椎病 - 听力损失 (CATSHL) 综合征是一种罕见的遗传性疾病.
- 以前的CATSHL综合征病例与特定的FGFR3变异有关.
关键词:
这就是CATSHL综合征.在FGFR3中.这就是LADD综合征.坎普托达克蒂利 (Camptodactyly) 是一个指甲状腺的疾病.听力障碍 听力障碍 听力障碍过度生长 过度生长脊柱体脊椎病是什么?脊柱体脊椎病是什么?更多相关视频
07:38Functional Characterization of Na+/H+ Exchangers of Intracellular Compartments Using Proton-killing Selection to Express Them at the Plasma Membrane
Published on: March 30, 2015
9.3K
05:51A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
25.9K
相关概念视频
Incomplete Dominance
22.6K
Gregor Mendel's work (1822 - 1884) was primarily focused on pea plants. Through his initial experiments, he determined that every gene in a diploid cell has two variants called alleles inherited from each parent. He suggested that amongst these two alleles, one allele is dominant in character and the other recessive. The combination of alleles determines the phenotype of a gene in an organism.
22.6K
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
Cohesins
4.5K
Cohesin protein complexes are a molecular glue that holds two sister chromatids together. They play an important role both in mitosis and meiosis. In mitosis, all cohesin complexes present on the chromosomes are removed before the start of the anaphase stage.
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of...
Cohesin complexes in Meiotic Division
Meiosis involves two distinct rounds of chromosomal segregation and cell divisions— Meiosis I followed by Meiosis II – producing four daughter cells. Meiosis I includes the separation of...
4.5K
Exon Recombination
3.6K
The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes.
Exon shuffling follows “splice frame rules.” Each exon...
Exon shuffling follows “splice frame rules.” Each exon...
3.6K
X-Inactivation
38.6K
The human X chromosome contains over ten times the number of genes as in the Y chromosome. Since males have only one X chromosome, and females have two, one might expect females to produce twice as many of the proteins, with undesirable results.
38.6K
Pedigree Analysis
84.3K
Overview
84.3K
