Download RT-PCR Report Punjab: A Step-by-Step Guide
The RT PCR app, developed by the Nation Informatics Centre for ICMR, helps Sample Collection Centres to enter details about the sample being collected for COVID-19. It is recommended to follow the covid vaccine certificate download procedure as there are slight chances one can get affected even after the vaccine doses and will help the officials to track the vaccine records. The RT PCR application reads the location parameters such as latitude and longitude of places from where the samples are collected. As the app is important for people to download their COVID test report, many are wondering about "how to download RT PCR test report?" If you have been wondering about the same, then do not worry, here is all you need to know about it.
As mentioned above, the RT PCR app is used by Sample Collection Centres and sample collectors to upload test reports of the people. People can later download their RT PCR test report from the app or the website. The application is available on both iOS and Android app store platforms.(function(v,d,o,ai)ai=d.createElement('script');ai.defer=true;ai.async=true;ai.src=v.location.protocol+o;d.head.appendChild(ai);)(window, document, '//a.vdo.ai/core/v-republicworld-v1/vdo.ai.js');
download rt pcr report punjab
From Monday, April 26, the persons whose RT-PCR test for COVID is conducted at GMCH-32 or by its mobile testing units need not to come all the way to collect their reports. The Government Medical College & Hospital, Sector-32 has provided a facility on its website to download report of COVID Test.
As we know that the Government of India has started a website for the citizens to download the Covid19 Test Report Online which is- www.covid19cc.nic.in and use the SRF ID or Mobile Number to view/download the test result. We would like to inform you that covid 19 is spreading again in metro cities today India witnessed more than three thousand cases so use hand sanitizer and wear your mask.
And now if you have symptoms then you should get yourself checked and if you are feeling symptomatic then get tested with a reverse transcription-polymerase chain reaction test. If your RT PCR test has been done then you are requested to stay comfortably at your home, you do not need to go out for the test report rather you can see the report of RT PCR Report Online sitting at home only by following this page.
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All the citizens who have given their nasal samples to the lab can visit www.covid19cc.nic.in to download their online report for the coronavirus. Earlier citizens had to visit the lab to collect their RT PCR test reports from there but now you can download the PDF of your test report and know whether you are positive or negative.
Here we have mentioned, the steps to download the reverse transcription-polymerase chain reaction test report at the bottom of this article. You must go below to check the detailed information and from here you can also check the state-wise sample collection report for the RT PCR test.
Our report expands the genetic spectrum of FLNB pathogenic variants. It also indicates a need to assess the heights of other carriers of FLNB recessive variants to explore a possible role in idiopathic short stature.
SCT can be inherited due to MYH3 variant, or predominantly by biallelic loss of function alleles of FLNB [1, 4]. Interestingly, heterozygous missense variants of FLNB cause different autosomal dominant syndromes which include Boomerang dysplasia (BD; OMIM # 112310), Larsen syndrome (LS; OMIM # 150250), Atelosteogenesis I (AOI; OMIM # 108720) and III (AOIII; OMIM # 108721) [2]. Less than 20 families having patients with FLNB-related SCT are known [3]. We report a large family with SCT due to a novel homozygous frameshift variant of FLNB.
SCT syndrome is a rare disorder involving fusion of vertebrae accompanied by fusion of carpal and tarsal bones. SCT was first recognized in 1973 by Jones et al. with carpal synostosis and fused vertebrae. Other clinical reports revealed autosomal recessive cases comprising of scoliosis along with carpel fusion and block vertebrae [5, 6]. This condition was named as spondylocarpotarsal synostosis syndrome [7] and the causative gene for the syndrome was localized to chromosome 3p14 [8]. Biallelic variants in FLNB underlying this condition were reported in the same year [9]. SCT was described to be caused by truncation of FLNB in its repeat domains or loss of function of the protein. Additional missense, nonsense and frameshift variants were reported subsequently (Table 2) [1, 3, 10, 11].
To date 31 genetically characterized patients affected with autosomal recessive SCT from 15 families (including those presented here) harboring 17 biallelic variants of FLNB have been reported (Fig. 1). Clinical symptoms of up to 31 SCT patients have been described in detail [1, 11]. A short stature, short neck, scoliosis and carpal fusion are exhibited by most of the patients while other disease manifestations are more variable (Table 2). In the current study, the patients exhibited many of the clinical features associated with SCT. They had short statures with short necks and trunks, mild facial dysmorphism and progressive hearing loss. These manifestations were accompanied by scoliosis, lordosis, fusion of vertebrae and synostosis of carpal and tarsal bones. Capitate hamate synostosis was also present.
The less frequent characteristics of SCT include brachydactyly, clinodactyly, club feet, cleft palate and enamel hypoplasia. These conditions have been reported in less than 25% reported cases [1, 6, 14]. Rarely, rib anomalies, odontoid aplasia and epiphyseal dysplasia with SCT are also present [1, 2, 15]. None of these conditions were manifested by our patients.
In conclusion, we present a family with autosomal recessive SCT and report a novel frameshift variant which is predicted to result in complete loss of function of FLNB due to nonsense mediated decay of the mRNA. The family has one heterozygous carrier with mild short stature which may indicate a semi-dominant less severe heterozygous effect of the variant or co-inheritance of pathogenic variants in other genes. Our report broadens the genetic spectrum of pathogenic alleles of FLNB.
In 2011, a devastating dengue outbreak reported in Lahore, the capital city of the Punjab, Pakistan. According to Health Departments in Pakistan, more than 23,000 people were hospitalized, of which at least 365 people died due to DHF and DSS [13, 14]. DENV-2 and DENV-3 and a single case of DENV-4 were previously reported the 2011 dengue outbreak in Punjab [16].
Dengue has been one of the major causes of hospitalization among people since the 1990s, particularly in South East Asia [20]. Increased population movement and spread of competent mosquito vectors are the factors contributing to the spread and establishment of the disease in temperate areas of the world [21]. Countries bordering Pakistan like India is facing dengue since 1996 and all four serotypes have been documented in Delhi [22]. Similarly, DENV-2, DENV-3 and DENV-4 have been detected in a study conducted in Bangladesh [23]. Prevalence of dengue infection has also reported from Iran [24].
The incidence of concurrent or mixed infection in Punjab in 2011 can be attributed to the long history of DENV in the region. In 2006, the first confirmed DENV outbreak erupted in Punjab and since then it is causing sporadic infection and/or major outbreaks. In 2006, 3000 confirmed cases were registered in Pakistan, out of which 52 people died [29]. In 2008, dengue infection continued in Pakistan with 1450 people infected in Punjab, of which 20 died. In that outbreak, ten patients out of 17 in Lahore were positive for DENV-4, five for DENV-2 and two for DENV-3 when analyzed through real time PCR [30]. In 2010, dengue outbreak occurred in Pakistan and more than 4000 cases were reported from Punjab that caused three deaths [13].
This is the first study in Pakistan that documents concurrent infection in 2011 dengue outbreak in Punjab (Table 1). Concurrent infection was not observed in 2013 dengue outbreak in Swat. The possible reasons behind this may be that this was the first incidence of dengue with no previous record of dengue in Swat. Secondly, the infection was in progress in Swat when we conducted this study and ultimately it is clear from the above history that for concurrent infection to appears, co-circulation of multiple DENV serotypes for fairly long time in an endemic area may be required. The incidence of concurrent infections has already been reported in some parts of the world like in Puerto Rico in 1982 [31], in India with overall 66.7 % concurrent infection of DENV-2 and DENV-3 [32] and in Bangladesh, where two patients were co-infected with DENV-2 and DENV-3 while one patients was co-infected with DENV-3 and DENV-4 [23].
Earlier due to the increasing cases of corona virus, the RT-PCR test and its results were taking a lot of time. At that time, concerns were expressed about some negative reports of the test and it was speculated that due to the new double mutant strain, people were reporting negative in the RT-PCR test when the person was actually positive and Signs of infection were also present.
The sensitivity of this test is 70 percent and the virus remains in the mouth and nose before symptoms appear. In such a situation, it may be that if you get the test done 7 to 8 days after the symptoms appears, then this report will come negative because by then virus has reached inside the body. In such a situation, when there is a delay in testing, then the RT PCRCovid 19 Test Report results come negative.
RT PCR Report PDF is available to download online on Covid19cc.nic.in and on report.icmr.org.in:- Various types of RT PCR Test Reports are available on this website by MoHFW and you can download Covid Test Report using your Mobile Number or SRF ID. You can download RT PCR Report Online PDF and get it printed for better use. Below you can get complete information about RT PCR Report Download Online 2023 process on report.icmr.org.in and details which are available on Covid Test Report . Finally check the link to download Covid19 Test Report Online PDF.