CN211112006U

CN211112006U - Deafness gene detector with sample information recognition device

Info

Publication number: CN211112006U
Application number: CN201921592164.2U
Authority: CN
Inventors: 高翊
Original assignee: Kunming Boao Three Medical Laboratory Co ltd
Current assignee: Kunming Boao Three Medical Laboratory Co ltd
Priority date: 2019-09-24
Filing date: 2019-09-24
Publication date: 2020-07-28
Anticipated expiration: 2029-09-24

Abstract

The utility model is suitable for a deafness gene diagnostic equipment technical field provides a deafness gene detector with sample information recognition device, including the detector body, the detector body has the sample inlet that is used for supplying the sample seat to insert, the sample inlet is located one side or the front of the detector body, the detector body is inside to be provided with gene detector in the sample inlet; one side of introduction port is provided with sample information identification device, sample information identification device is radio frequency chip and reads module or NFC identification module, and the side of sample seat is provided with radio frequency chip or NFC chip, the side of detector body is provided with print module. The utility model provides a deafness gene detector with sample information recognition device, it has improved operating efficiency, easy operation and automation are efficient.

Description

Deafness gene detector with sample information recognition device

Technical Field

The utility model belongs to the technical field of deafness gene diagnosis equipment, especially, relate to a deafness gene detector with sample information recognition device.

Background

Deafness is one of the most common clinical hereditary diseases, and accounts for about 60% of the cases caused by hereditary factors, and the second sampling investigation of Chinese disabled people in 2006 shows that the total number of the disabled people is 8 million, the hearing disabled people are 2670 million, about 80 million hearing-impaired children are 1-7 years old, and the incidence rate of serious hearing impairment is 1-3 per thousand in 2000 million newborn children per year in China. In non-syndromic deafness, autosomal recessive inheritance accounts for about 75-85%, autosomal dominant inheritance accounts for 12-13%, X-linked inheritance accounts for 2-3%, and Y-linked inheritance, mitochondrial inheritance, etc. are also included. The gene mutation identification method has great clinical value for finding and detecting deafness-causing genes, can be used for etiological diagnosis, genetic consultation, prenatal diagnosis and newborn hearing screening of deafness patients, and can help and remind doctors to use specific antibiotics with caution so as to avoid deafness of children carrying gene mutation.

According to the related documents and the report of academic conference of the research team of the national deafness project, about 21% of deafness patients have GJB2 gene mutation, 14.5% of deafness patients have S L C26A4 gene mutation, and 3.8% and 0.6% of deafness patients have mitochondrial DNAA1555G and C1494T mutation respectively, the result reveals that the occurrence frequency of common deafness mutation of Chinese deafness patients is determined, and the GJB2, S L C26A4 and mitochondrial gene 12SrRNA (A1555G and C1494T mutation) are three most common genes causing most genetic deafness in China, about 70-80% of genetic deafness individuals are caused by the mutation of the three genes, under the support of a large amount of clinical detection data, 20 deafness gene mutation sites listed as detection targets can cover most deafness gene mutation sites, and simultaneously, the ratio of the genetic mutation sites related to the hereditary deafness is about 4832, and the ratio of the genetic mutation sites related to the genetic clone genes is about 582 after the congenital deafness in China.

In recent years, genetic diagnosis kits of congenital deafness genes or susceptibility deafness genes, and detection devices and methods thereof have been reported in China successively, for example, CN201610942873.3 genetic deafness gene mutation detection kit, CN201110455939.3 detection device for gene detection, CN201680069509.9 PNA probe for detecting genetic deafness, and method for detecting genetic deafness using the probe, etc., so as to meet the requirement of carrying out extensive screening on deafness-related gene mutations.

SUMMERY OF THE UTILITY MODEL

An object of the utility model is to overcome above-mentioned prior art not enough, provide a deafness gene detector with sample information recognition device, its easy operation and automatic efficient.

The utility model discloses a realize like this: a deafness gene detector with a sample information recognition device comprises a detector body, wherein the detector body is provided with a sample inlet for inserting a sample seat, the sample inlet is positioned on one side or the front side of the detector body, and a gene detector is arranged in the detector body at the sample inlet; one side of introduction port is provided with sample information identification device, sample information identification device is radio frequency chip and reads module or NFC identification module, and the side of sample seat is provided with radio frequency chip or NFC chip, the side of detector body is provided with print module.

Specifically, the top of the detector body is provided with a display.

Specifically, the display is connected to the top of the detector body through a rotating shaft structure.

Specifically, the sample information recognition device is provided with a status indicator lamp.

Specifically, this internal wireless communication module that is provided with of detector.

The utility model provides a deafness gene detector with sample information recognition device, it has improved operating efficiency, easy operation and automation are efficient.

Drawings

In order to more clearly illustrate the technical solutions in the embodiments of the present invention, the drawings needed to be used in the embodiments will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art that other drawings can be obtained according to these drawings without creative efforts.

FIG. 1 is a schematic perspective view of a deafness gene detector having a sample information recognition device according to an embodiment of the present invention;

fig. 2 is a schematic plan view of a deafness gene detector having a sample information recognition device according to an embodiment of the present invention.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more clearly understood, the present invention is further described in detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.

It will be understood that when an element is referred to as being "secured to" or "disposed on" another element, it can be directly on the other element or intervening elements may also be present. When an element is referred to as being "connected to" another element, it can be directly connected to the other element or intervening elements may also be present.

It should be noted that the terms of orientation such as left, right, up and down in the embodiments of the present invention are only relative to each other or are referred to the normal use state of the product, and should not be considered as limiting.

As shown in fig. 1 and fig. 2, an embodiment of the present invention provides a deafness gene detector with a sample information recognition device, which includes a detector body 100, wherein the detector body 100 has a sample inlet 110 for inserting a sample holder (kit), the sample inlet 110 is located on one side or the front side of the detector body 100, and a gene detector is disposed inside the detector body 100 at the position of the sample inlet 110; one side of introduction port 110 is provided with sample information recognition device 210, sample information recognition device 210 reads module or NFC identification module for the radio frequency chip, and the side of sample seat can correspond and be provided with radio frequency chip or NFC chip, the side of detector body 100 is provided with print module, and like this, when examining, only need insert introduction port 110 with the sample seat, sample information that sample information recognition device 210 can prestore in synchronous discernment radio frequency chip or the NFC chip, it can include the identity information of sample, for example name, age, sample acquisition time, the collection place, also can be including the detection type that will go on etc., operating personnel need not other actions of typeeing, and the operating efficiency is greatly improved, and easy operation and automation efficiency are high, and the testing result can automatic printing.

Specifically, a display is disposed on the top of the detector body 100, and the display may be a touch screen for easy viewing and operation.

Specifically, the display is connected to the top of the detector body 100 through a rotating shaft structure so as to be folded and folded.

Specifically, the sample information recognition device 210 is provided with a status indicator light, and after the information is read, the status indicator light can be green, and after the sample holder is pulled out, the status indicator light can be red.

Specifically, a wireless communication module is disposed in the detecting instrument body 100, and the detecting result and the information of the sample information identifying device 210 can be uploaded to a server through the wireless communication module for archiving and backup.

Specifically, the gene detector can detect genes such as GJB2, GJB3, S L C26A4 (PDS for short), mtDNA12srRNA (mitochondrial gene), and the like, thereby diagnosing deafness.

Specifically, an ultraviolet lamp device may be disposed in the detector body 100 to prevent the reagent cartridge (sample) from being contaminated.

Specifically, the sample information identifier 210 may be connected to a circuit board in the apparatus body 100 by a cable.

Specifically, the inside of introduction port 110 is provided with the control by temperature change part to make the temperature of sample unified, do benefit to and improve and detect the precision.

Specifically, a temperature sensor is disposed at the injection port 110, and the temperature sensor and the temperature control component may be electrically connected to the main board.

Specifically, the temperature control component is a semiconductor refrigeration device, and the temperature can be reduced and increased by controlling the current direction.

The utility model provides a deafness gene detector with sample information recognition device, it detects conveniently, and easy operation and automation are efficient.

The above description is only exemplary of the present invention and should not be taken as limiting the scope of the present invention, as any modification, equivalent replacement or improvement made within the spirit and principle of the present invention should be included in the present invention.

Claims

1. A deafness gene detector with a sample information recognition device is characterized by comprising a detector body, wherein the detector body is provided with a sample inlet for inserting a sample seat, and a gene detector is arranged in the detector body at the sample inlet; one side of introduction port is provided with sample information identification device, sample information identification device is radio frequency chip and reads module or NFC identification module, and the side of sample seat is provided with radio frequency chip or NFC chip, the side of detector body is provided with print module.

2. The deafness gene tester with sample information identification device of claim 1, wherein a display is disposed on the top of the tester body.

3. The deafness gene tester with sample information identification device of claim 2, wherein said display is connected to the top of said tester body by a hinge structure.

4. A deafness gene tester according to any of claims 1 to 3, wherein the sample information identification means is provided with a status indicator light.

5. The deafness gene detector of any of claims 1-3, wherein the detector body has a wireless communication module disposed therein.