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Basic Genetic Evaluation in Obstetrics PowerPoint Presentation

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This medical PowerPoint presentation talks about Genetic evaluation in obstetrics. Genetic evaluation in obstetrics involves assessing the risk of genetic disorders or abnormalities in a fetus or newborn.

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Published on : Mar 21, 2023 | Views : 1443 | Downloads : 1

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Slide 1-

Basic genetic evaluation in obstetrics Yashodhara Pradeep Professor Dept of Ob Gyn King George Medical University Lucknow
Slide 2-

Obstetrician Gynecologist as Primary Genetic Counselors Initiation of genetic counseling Explain the Risk Options for Genetic Testing Referral to Genetic consultants
Slide 3-

Basic Genetic Evaluation Medical genetics is the investigation of individual variation in the incidence of susceptibility to disease, as well as disease mechanism, response to therapy, and results of tests. 2-3 % Children born with a congenital birth defect, by age 18 Approximately 8% are discovered to have one or more anomalies 2/3 of population will experience a disease with a genetic component in their lifetime and if cancer included it is 91%
Slide 4-

Family Medical History Spinal muscular atrophy ( SMA) Autosomal recessive neuro muscular disorder mutation in SMN1 gene 1:10,000 birth carrier frequecy 1:53 in Asians Carrier screening for Hemoglobinopathies Cystic Fibrosis Thrombophilias Fragile X syndrome (pre mutation FMR1 gene ) Potential genetic risk to offspring
Slide 5-

Referral to genetic counselor Minimal Information to be given: Indication for referral Significant Medical History along with pertinent laboratory test results Role of Genetic professionals Analysing pedigree data of three generations (family information) risk assessment, tests offered, patients uptake of testing, interpretation of results molecular and genetic tests & provides genetic counseling and prenatal diagnosis, follow up plan along with consultation summary
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Genetics In Obstetrics Chromosomal Abnormalities Single Gene ( Mendelian ) Disorder Non Mendelian Patterns of Inheritance Molecular Genetics
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Types & Frequency of Genetic Disease Chromosomal Disorder: 1.8 4 Single gene disorder 3.6 20 Multifactorial disease 48.4 646 Somatic cell genetic disorder ( cancer ) 240 Total 906/1000
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Chromosomal disorder Chromosomal disorders are numerical and structural Duplication or deletion of chromosome or part of chromosome can be associated with severe outcomes like mental retardation , minor or major structural defects Balanced chomosomal rearrangements like reciprocal translocation or an inversion are not associated with phenotypic abnormalities total DNA content is not altered Conceptus with major chomosomal imbalance are spontaneously aborted Disorders caused by deletions cannot be diagnosed by traditional cytogenetic techniques , they require FISH eg Prader-willi syndrome, Angelman syndrome, William syndrome
Slide 9-

Chromosomal Abnormalities Standard Nomenclature Aneuploidy Paternal Defects Autosomal Trisomies Sex Chromosome Abnormalities Chromosomal Translocations Chromosomal Deletions Chromosomal Inversions Ring Chromosomes Chromosomal Mosaicism
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Nomenclature Aneupolidy: Most common & easily recognizable Numerical anomalis : N 46 XX or 46 XY 47 XX 47 XY,+21/46XY 46XY,del(4)(p14) Trisomy 21, 13, 18 Monosomy Turner syndrome 47XXX, 47XXY, 47XYY, Polyploidy, Triploidy, Tetra ploides
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Chromosomal translocations Reciprocal translocations Robertsonian translocations Isochromosomes 2q or2 p are fused together
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Chromosomal Mosaicism Two or more cytogenetically distinct cell lines in the same individual. Mosaic Down Syndrome one cell line with 47 chromosomes and a normal cell line with 46 chromosomes Phenotypic expression depends on many factors involvement of only placenta, both placenta & fetus or fetus only Gonadal Mosaicism as a result of meiotic error in zygote Achondroplasia, Osteogenesis imperfecta, X linked disease Duchenne muscular dystrophy
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Single gene disorder Disorder caused by defect (mutation) single gene or monogenic disorder Follow Mendelian principles of inheritance More than 5000 monogenic disorders are identified These disorders are caused by various genes on autosomes, sex chromosomes, or on the mitochondrial genome Monogenic disorders involving each system of the body, some of them predominantly involve one system of body eg. Thalassaemia, haemophilia, achondroplasia Monogenic disorders involveing many systems of body are mucopolysaccharidosis, galactosemia, and mitochondrial disorders
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Single gene ( Mendelian ) Disorder Autosomal Dominant Autosomal Recessive Consanguinity Co- Dominant Genes X-linked & Y –linked Genes The advance knowledge of pathogenesis of disease tells no disease is monogenic many other genes and environmental factors interact with diseases causing gene and modify the phenotype
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Single gene Mendelian Disorder Autosomal Dominant : Achondroplasia, Acute intermittent porphyria, Adult polycystic kidney disease, BRACA1, BRCA2 Breast cancer, Familial hypercholesterolemia , Familial hypertrophic cardiomyopathy, Marfan syndrome, Huntington chorea , Myotonic dystrophy, Neurofibromatosis, etc Autosomal Recessive : Albinism, Cystic fibrosis, Deafness, Sickle cell Anemia, Beta Thalassemia, inborn errors of Metabolism X linked Chronic granulomatous disease, color blindness, Fragile X syndrome, Hemophilia A& B, Testicular Feminization Risk of recurrence depends upon penetrance, variable expressivity, anticipation
Slide 16-

Characterestic of inheritance Autosomal Dominant: Successive or multiple generations are affected Both males and females are effected in equal proportions Both males and females can transmit the disease to their offspring of either sex Risk of recurrence 50 % Examples ----Achondroplasia, Acute intermittent porphyria, Adult polycystic kidney disease, BRACA1, BRCA2 Breast cancer, Familial hypercholesterolemia , Familial hypertrophic cardiomyopathy, Marfan syndrome, Huntington chorea , Myotonic dystrophy, Neurofibromatosis, etc
Slide 17-

Autosomal recessive : Both males and females are affected Disorder normally occurs in only one generation, usually with in single sibship The parents can be consanguineous especially if the dis order is rare Risk of recurrence parents are obligate carriers, the risk of second child being affected is 25%, 50% will be carriers, high chance of relatives are carrier If heterozygous of an autosomal disorder marries a normal person 50% of his children will be hetrozygous like him but there is no risk of having any affected child
Slide 18-

Common AR diseases are Albinism Congenital adrenal hyperplasia Cystic fibrosis Deafness Friedreich ataxia Homocystinuria Hemochromatosis Thalassemia Syndrome Sickle cell Anemia Phenylketonuria ( In born error of metabolism ) Taysachs diseases
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Consanguinity and Autosomal recessive inheritance Consanguineous couple means having common ancestor in preceding five generations, the likelihood of their inheriting an identical allele ( from their common ancestor) and passing it to their child is high Sharing of Genes Mating between third degree relatives who share 1/16 of genes EX mating between first cousin, a half uncle or aunt, a half niece or nephew or more distantly related individual More common to produce Autosomal recessive or multifactorial diseases like osteoporosis (3-17%), Thalassaemia major (2-3%)
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X-linked inheritance It is due to the presence of recessive genes on Xchromosomes Females are carriers as homozygous mutations are rare Males are affected almost exclusively All affected males are related through unaffected females (carriers) Male to male transmission is never observed because the X-chromosome in a male is always contributed by mother An effected male can pass on the disorder to his grandsons through his unaffected carrier daughter Risk of Recurrence is variable 50% will be affected, 50% daughter will be carrier, Mother carrier father affected, Father is affected Mother is carrier
Slide 21-

Non Mendalian Patterns of Inheritance Hereditary Unstable DNA Imprinting Uniparental Diasomy Mitochondrial Inheritance Polygenic and Multifactorial Inheritance
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Non Mendelian Patterns of Inheritance Fragile X syndrome Myotonic Disorder Huntington disease
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Molecular Genetics Organization of the Genomes Coding DNA Control OF Gene Expression New Mutations and Gene REGULATION Non Coding DNA Genetic Tests
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Genetic Test Cyto genetic tests FISH Spectral Karyotype Analysis Linkage analysis RELPs, STRs Complementary DNA Fluorescence- activated Chromosome sorting Gel separation PCR Southern blot MLPA
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Types of Problems in Morphogenesis Malformation Deformation Disruption
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Preconceptional Counseling Diet & Nutrition Risk reduction Review of medication for potential teratogenicity Review of immunization Cessation of Smoking Control of Diabetes Control of HT Control of Infections eg UTI, PTB, Control of Anemia Detection of HBSAg , HCV, HIV, VDRL