dystrophy造句

1、fascioscapulohumeral dystrophy

2、He had muscular dystrophy.

3、infantile neuroaxonal dystrophy

4、duchenne muscle dystrophy

5、hyperplastic dystrophy of vulva

6、Clinical for muscular dystrophy, myasthenia gravis, muscular dystrophy, polymyositis, motor neuron disease, such as atrophy disease syringomyelia.

7、My son is suffering from muscular dystrophy.

8、There's currently no cure for any form of muscular dystrophy.

9、The FacioScapuloHumeral Muscular Dystrophy Society addresses issues and needs related to this disease of the skeletal muscle, which is a type of muscular dystrophy.

10、Objective Perform gene diagnosis for Chinese facioscapulohumeral muscular dystrophy (FSHD).

11、Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy (FSHD) 1A gene.

12、Objective:This paper was to find the susceptive gene of limb girdle muscular dystrophy (LGMD) in Chinese.

13、Most children with Duchenne muscular dystrophy die in their late teens or early 20s.

14、Since cell growth is a fundamental biological process, the research may shed light on everything from miscarriages to muscular dystrophy.

15、Objective To investigate the clinical and lab features of sibling brother and sister both with Duchenne muscular dystrophy (DMD).

16、Muscular dystrophy is a group of more than 30 genetic diseases, characterized by progressive weakness and deterioration of skeletal muscles.

17、Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.

18、Gastrodia Expelling Wind and patch Main indications: liver and kidney weakness, Meridian dystrophy, hypertension, headache, hand and foot numbness, lumbar and leg pain.

19、Like other X-linked disorders such as color blindness and muscular dystrophy, genetic mutation causing a son's infertility could be passed from his mother.

20、Wilson'disease was often misdiagnosed as various kinds of hepatitis, lunacy, falling sickness, arthritis, muscular dystrophy, nephritis, et al, with the misdiagnosis rate of 55.5%.

21、Visual field analysis is interfered by HM fundus dystrophy, also relationship with study curve, long wave motion and short wave motion.

22、Objective To provide a useful tool based on molecular level for clinical diagnosis and classification by detecting gene products encoded by disease genes of muscular dystrophy.

23、a severe form of muscular dystrophy marked by facial weakness and drooping eyelids and difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips.

24、Inherited gene mutations, such as those that cause hemophilia or muscular dystrophy, would have to be corrected as well before using a patient's own cells to create ES cells.