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kindly review with clinical findings
कृपया नैदानिक निष्कर्षों के साथ समीक्षा करें
Last Update: 2023-04-21
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kindly review and confirm on the same
कृपया इसके लिए पुष्टि करें
Last Update: 2024-05-04
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unfortunately , it is not a clean , quantifiable system that can help you predict the prakriti with clinical precision .
दुर्भाग्यवश यह स्वच्छ और परिमाणांकनीय प्रणाली नहीं है जो नैदानिक परिशुद्धता के साथ प्रकृति के विषय में भविष्यवाणी करने में आपकी कुछ मदद कर सके ।
Last Update: 2020-05-24
Usage Frequency: 1
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mrna-based vaccine candidate bnt162, currently in pre-clinical testing with clinical trials expected to begin in april 2020.
mrna-आधारित टीका उम्मीदवार bnt162, वर्तमान में पूर्व-नैदानिक परीक्षण में है, जिसके नैदानिक परीक्षण अप्रैल 2020 में शुरू होने की उम्मीद है।
Last Update: 2020-08-25
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thank you so much for taking the time to leave us this amazing review.” “we are so grateful for your kind words. thanks for sharing your review with us and the community.”
Last Update: 2020-06-19
Usage Frequency: 1
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dna test report– medgenome laboratories patient and order details order id : 840273 order date : 25-01-2024 date of report : 10-02-2024 full name age/gender sample id sample type collected on received on hitesh odidera 19y/male 8318487 peripheral blood in edta 20-01-2024 23-01-2024 referring clinician : dr. jacky ganguly, institute of neurosciences, (kolkata) requested test : additional family member (investigational) testing - 1 variant (mgm277) clinical diagnosis / symptoms / history the index patient, khunti ranabhai k, born of a non-consanguineous marriage, presented with clinical indications of slowly progressive neck jerks (since 8 years of age), hand jerks while writing and holding objects, myoclonus, dystonia, telangiectasia and anxiety. there is a profound family history of similar complaints in his with multiple affected individuals. mr. khunti ranabhai k. is suspected to be affected with myoclonus dystonia syndrome. khunti ranabhai k was found to harbour a heterozygous variant of uncertain significance, c.1796_1798dup in the ano3 gene. cousin of the index patient is being evaluated for the same variant. result summary analysis for the variant detected by next generation sequencing in the ano3 gene of index patient, khunti ranabhai k (sample id:8185923) name : hitesh odidera/male/19y relationship to the index patient : cousin sample id : 8318487 gene name exon / intron variant reported in the index patient variant detected in family member* clinical condition of family member ano3 exon 17 chr11:g.26599674_26599676du p; c.1796_1798dup (het); (p.ala599dup) present & heterozygous symptomatic * the variant analysis in sanger sequencing is based on the ano3 gene reference sequences enst00000256737.8 (grch38) [1]. the exon number and nucleotide numbers will differ based on the reference file chosen and the database used. interpretation a heterozygous 3 base pair insertion in exon 17 of the ano3 gene [chr11:g.26599674_26599676dup; c.1796_1798dup; (p.ala599dup)] was detected in the index patient by ngs (sample id: 8185923; repo
Last Update: 2024-02-11
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