Genetic Disorder - Achondrogenesis скачать в хорошем качестве

Genetic Disorder - Achondrogenesis

Achondrogenesis is a group of severe disorders that are present from birth and affect the development of cartilage and bone. Infants with achondrogenesis usually have a small body, extremely short arms and legs, other skeletal abnormalities, and underdeveloped lungs. symptoms that people with this disease may have:- Abnormality of bone mineral density Abnormal endochondral ossification Anteverted nares Aplasia/Hypoplasia of the lungs Diagnosis of Achondrogenesis may be suspected by symptoms but is confirmed by genetic testing. Genetic testing for finding the mutation in this gene is of high importance to know the exact cause and prognosis of the disease. Genetic testing also helps doctors to determine the most suitable treatment plan with the least adverse effects. Genetix.us offers genetic testing from the world's most advanced laboratories for accurate diagnosis of Achondrogenesis to help doctors with better insight into this disease. Apart from genetic testing, our services include medical consultations from some of the top experts in the USA based upon the test reports. These tests are available through our partnering clinics in USA, UAE and India. For more details, please visit our website or send a whatsapp message to + 1- (913) 592-9696 #Dubai #India #USA #geneticdisorder #geneticdiseases #genes #geneticstudy #genetics