网络中风的家族史;中风家族史 网络释义 1. 中风的家族史 ICD 10... ... Z823Family history of stroke中风的家族史Z8241 Family history of sudden cardiac death 心脏性猝死的家族史 ... icd-10th.blogspot.tw|基于 1 个网页 2. 中风家族史
Introduction:The role of genotype in sudden cardiac death (SCD) risk stratification in hypertrophic cardiomyopathy (HCM) patients is unclear. Whether family history of SCD (FHxSCD) is independently associated with SCD after correction for genotype has never been investigated.#Methods:This observational ...
No family history of convulsion and sudden cardiac death for three generations was evident. She had undergone cochlear implant surgery. Her resting 12 lead ECG showed prominent prolongation in QTc distance of 530 ms (Fig. 2b). Propranolol was commenced at a dose of 0.004 g/kg four times in ...
The observed consistency with published results from the Savanna Pume hunter-gatherers, a distinct group with a different evolutionary history, supports the notion that the adiposity rebound does not apply to hunter-gatherer populations at large. Subsequent research on other self-sufficient populations ...
To the best of our knowledge, this is the first case report of a patient who has BrS with a history of sudden death in four first-degree family members. Studies reporting sudden deaths of one first-degree relative of patients with BrS are common; however, the number of reports of sudden...
Patient was scheduled to undergo ambulatory ECG monitoring every 3 months with subsequent restratification for ICD implantation at 6–12 months time. Because of the family history (apical LV aneurysm in the patient's aunt, ventricular arrhythmias in the patient's aunt and father), presence of ...
[20] have provided a comprehensive over- view of the evolutionary history of MAPKs in green plants by using a limited number of plants species. However, there is currently limited information regard- ing the nomenclature, conserved structures, genomics and biochemistry of MAPKs in plants. In ...
Five generations of the family had a long history of sudden cardiac death and cardiac problems. ANM_ 000257.4:c.2342T>A (p.Leu781Gln) variant was detected in the MYH7 gene. It was heterozygous in the proband and in all affected individuals in a large family. Th...
A thorough familial history was obtained, revealing a deceased father at the age of 41 (due to presumed sudden cardiac death, SCD), a deceased brother at the age of 47 years old (SCD), and a 54-year-old brother diagnosed with heart failure of unknown etiology more than 10 years ago. ...
The patient has two daughters, one of whom was diagnosed with apical hypertrophic cardiomyopathy at the age of 26. Due to the genetic findings, the mother of his two daughters was also genetically evaluated and studied. The family history of both branches of the family was extensively ...