مولکولی و پانل بیماری ها

  • پانل بیماریهای ناباروری مردان، زنان و سقط های مکرر

 

:Male infertility

Karyotype Analysis

Y microdeletion (AZFa, AZFb, AZFc)

Cystic Fibrosis (CF)

Kallmann Syndrome

Androgen Insensitivity Syndrome (AR)

5-alpha Reductase Deficiency (SRD5A2)

Leydig Cell Hypoplasia (LHCGR )

Male Infertility NGS Panel

 

 

:Female infertility and Recurrent abortion

Karyotype Analysis

Fragile X Syndrome (POF)

Congenital Adrenal Hyperplasia

Kallmann Syndrome

Perrault Syndrome

Ovarian Dysgenesis (BMP15)

Ovarian Hyperstimulation Syndrome (FSHR)

Oocyte Maturation Defect (ZP1)

MullerianAplasia and Hyperandrogenism (WNT4)

Blood Coagulation Factors

Female Infertility NGS Panel

 

 

  • جدول پانل بیماریهای ژنتیکی همراه با تعداد ژنهای مورد آنالیز

 

 

Genes / Descriptiosn

Disease / Service Name

Row

Includes 219 genes

Genetic Testing for Disorders of Sex Development

    1   

Includes 514 genes

Genetic Testing for Intellectual Disability

    2    

Includes 463 genes

Genetic Testing for Short Stature

     3    

Includes 363 genes

Genetic Testing for Hereditary Skeletal Disorders

     4    

Including 278 genes

Genetic Testing for Monogenic Diseases In Muscular, Skeletal AndNervous Systems

     5    

Includes 355 genes

Genetic Testing for Renal Disorders

     6   

Including 164 genes

Genetic testing for Elderly Patients in Nervous System

     7   

Including 175 genes

Genetic Testing for Inherited Eye Diseases

     8   

Including 127 genes

Genetic Testing for Hearing Impairment

     9   

Including 118 genes

Genetic Testing for Inherited Metabolic Disorders

    10  

Including 96 genes

Genetic Testing for Monogenic Disorder In Skin System

    11  

Including 10 genes

Genetic Testing for Monogenic Disorder In Digestive System

    12  

Including 42 genes

Genetic testing for Monogenicdiabetes

    13  

Including 32 genes

Genetic testing for Immunodeficiency

    14  

Including 61 genes

Genetic Testing for Inherited Arrhythmias/Cardiovascular diseases

    15  

Including 58 genes

Genetic Testing for Diseases InEndocrine‐Urinary‐Blood‐Immune

System

    16  

Including 11 genes

Genetic testing forIdiopathic Hypogonadotropic Hypogonadism

    17  

Male/Female

Genetic Testing for infertility

   18  

Including 41 genes

Related to 15 cancers

Male Hereditary Cancer Panel

19

Including 49 genes

related to 16 cancers

Female Hereditary Cancer Panel

20

Including 21 genes

Breast / Ovarian Cancer

21

Including all genes in this system (244 genes+ MT‐DLOOP region)

Genetic testing for Mitochondrial Diseases

   22

30 M reads (3Gb of Data)/ 60 M reads (6Gb)

RNA‐SeqIlluminaPlateform, Truseq RNA

   23

Sequencing of more than 20 000 humangenes with clinical analysis of more than2700 genes (OMIM panel), related to morethan 4100 human genetic disorders.

Human Whole Exome Sequencing

   24 

                    -

Human Whole Genome Sequencing

   25  

Analyiss of deletions and duplications with

size > 100Kb, plus translocations, and

inversions analysis.

Chromosome Sequencing / Analysis

   26  

                    -         

Array CGH / Microarray Genotyping

   27  

.

 

 

 

 

 

 

 

آدرس : تبریز - خیابان ارتش - خیابان باغشمال - ساختمان میلاد / طبقه اول (مرکز مشاوره) / طبقه چهارم (آزمایشگاه) / طبقه ششم (واحد تحقیقات و توسعه)   ساعات پذیرش : 8 الی 21

تلفن طبقه اول : 35539273 - 41 - 98+            تلفن طبقه چهارم : 35574760 - 41 - 98+            تلفکس :  35574761 - 41 - 98+              ایمیل : info@mcllab.com

کلیه حقوق این سایت متعلق به مرکز مشاوره و آزمایشگاه بالینی ، سلولی و مولکولی میلاد می باشد.

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