'Prenatal diagnosis' diaporamas de présentation

Christian Morality

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2 pt

Types of mutations. Sex-linked Genetics. Genetic Disorders. Blood typing. Grab bag. 1pt. 1 pt. 1 pt. 1pt. 1 pt. 2 pt. 2 pt. 2pt. 2pt. 2 pt. 3 pt. 3 pt. 3 pt. 3 pt. 3 pt. 4 pt. 4 pt. 4pt. 4 pt. 4pt. 5pt. 5 pt. 5 pt. 5 pt. 5 pt.

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Gene 210 Fetal/Prenatal Sequencing

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Dr . Muhammad Rafique Assist. Prof. Paediatrics College of Medicine K K U Abha K S A

Dr . Muhammad Rafique Assist. Prof. Paediatrics College of Medicine K K U Abha K S A. PRENATAL DIAGNOSIS. It introduces option for management. From interruption of abnormal pregnancies to prepare for specialized peri-natal care. PRENATAL Dx.------CONT. Methods of prenatal diagnosis :

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BREAKING NEWS!

438 views • 33 slides

Prenatal Screening & Testing

Prenatal Screening & Testing. 5 March 2014 Rels 300 / Nurs 330. Prenatal Screening vs. Prenatal Diagnosis. Screening: aim is to identify women who have increased risk factors (larger than the general population of pregnant women) for having a child with a congenital anomaly

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Human Genome Project Gene Therapy

Human Genome Project Gene Therapy. Chapter 10 BIT 120. Human Genome Project. Begun in 1990, the U.S. Human Genome Project is a 13-year effort coordinated by the Department of Energy and the National Institutes of Health. Human Genome Project video. Goals of the Project.

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THALASSAEMIA

THALASSAEMIA. Konstantinidou Eleni Siligardou Mikela-Rafaella. THALASSAEMIA. The thalassaemias are a group of inherited hematological disorders caused by defects in the synthesis of one or more of the hemoglobin ( Hb ) chains.

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Phenylketonuria (PKU)

Phenylketonuria (PKU). Sanketh Proddutur. What is PKU?. Phenylketonuria (PKU) is an inherited error of metabolism caused by a deficiency in the enzyme phenylalanine hydroxylase (PAH). phenylalanine hydroxylase converts the amino acid phenylalanine to tyrosine, another amino acid . . Pathology.

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Chromosome Disorders

Chromosome Disorders. Prenatal Diagnosis. Amniocentesis. A small sample of the amniotic fluid surrounding the baby is removed using a syringe. The fluid contains skin cells from the baby. The skin cells are grown in the lab.

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Shoukhrat Mitalipov

Mitochondrial genome r eplacement in unfertilized o ocytes for t reatment of inherited mtDNA disease . Shoukhrat Mitalipov. Diseases caused by mtDNA mutations. There are more than 700 known disease-associated mtDNA mutations ( mitomap.org ) : - 285 tRNA / rRNA

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Creating a Welcoming Path for People with Special Needs

Creating a Welcoming Path for People with Special Needs. Roberta Witte Sacred Heart, Saratoga. Overview. Is my parish welcoming to all? Where do I begin? How can our parish do this? . Who are they?. Are families missing out on Mass and the Sacraments due to special needs?

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Audit of peripartum care

CWIUH 25.2.2010 Bridgette Byrne Senior Lecturer in Obstetrics and Gynaecology, RCSI and CWIUH. Audit of peripartum care. Audit of severe maternal morbidity and major obstetric haemorrhage. Near miss maternal morbidity. Lynch et al IMJ May 2008.

290 views • 17 slides

Christiane Theda MD PhD (FMH and Melbourne, Australia)

Introduction to the ALD Newborn Screening Study to be performed at Frederick Memorial Hospital and three other Maryland Hospitals PART 1: BACKGROUND INFORMATION. Christiane Theda MD PhD (FMH and Melbourne, Australia)

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13.3- The Human Genome

13.3- The Human Genome. What is a genome?. Genome: the total number of genes in an individual. Human Genome- approx. 20,000 genes on the 46 human chromosomes. Human Genome Project (HGP) Ongoing effort to completely map and sequence our genome. Human Genome Project.

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Primary Immunodeficiency Diseases

Primary Immunodeficiency Diseases. Primary immunodeficiencies are those in which the defect is intrinsic to the immune ?system, meaning it is genetically determined. Chronic Granulomatous Disease (CGD)

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Edwards Syndrome (Trisomy 18) by: Karen Guzman

Edwards Syndrome (Trisomy 18) by: Karen Guzman. What is Edwards Syndrome?.

439 views • 8 slides

Neurofibromatosis

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