Cardiofaciocutaneous genetic down syndrome. Medical search. Frequent questions

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Anatomy5

Chromosomes, Human, Pair 21 Chromosomes, Human, 21-22 and Y Nasal Bone Brain Neck

Diseases42

Down Syndrome Costello Syndrome Noonan Syndrome Facies Skin Abnormalities LEOPARD Syndrome Failure to Thrive Ectodermal Dysplasia Abnormalities, Multiple Syndrome Trisomy Metabolic Syndrome X Leukemia, Megakaryoblastic, Acute Fetal Diseases Nephrotic Syndrome Sjogren's Syndrome Intellectual Disability Turner Syndrome Nondisjunction, Genetic Williams Syndrome Myelodysplastic Syndromes Cushing Syndrome Heart Defects, Congenital Disease Models, Animal Acute Coronary Syndrome Polycystic Ovary Syndrome Chromosome Disorders DiGeorge Syndrome Horner Syndrome Craniofacial Abnormalities Prader-Willi Syndrome Long QT Syndrome Heart Septal Defects Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Alzheimer Disease Duodenal Obstruction Compartment Syndromes Tourette Syndrome Antiphospholipid Syndrome Porcine Reproductive and Respiratory Syndrome Klinefelter Syndrome

Chemicals and Drugs7

Estriol alpha-Fetoproteins Pregnancy-Associated Plasma Protein-A Chorionic Gonadotropin, beta Subunit, Human GATA1 Transcription Factor Biological Markers Chorionic Gonadotropin

Analytical, Diagnostic and Therapeutic Techniques and Equipment15

Facies Prenatal Diagnosis Amniocentesis Abortion, Eugenic Karyotyping Nuchal Translucency Measurement Ultrasonography, Prenatal False Positive Reactions Disease Models, Animal Case-Control Studies Risk Factors Genetic Testing Retrospective Studies Pedigree Prevalence

Psychiatry and Psychology4

Intellectual Disability Stanford-Binet Test Alzheimer Disease Tourette Syndrome

Phenomena and Processes14

Chromosomes, Human, Pair 21 Trisomy Maternal Age Pregnancy Trimester, Second Pregnancy Chromosomes, Human, 21-22 and Y Nondisjunction, Genetic Pregnancy, High-Risk Pregnancy Trimester, First Phenotype Paternal Age Mutation Mosaicism Gestational Age

Information Science1

Named Groups1

Infant, Newborn

Health Care6

Maternal Age Case-Control Studies Risk Factors Genetic Testing Retrospective Studies Prevalence

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Named Groups Health Care

Down Syndrome Costello Syndrome Noonan Syndrome Facies Skin Abnormalities LEOPARD Syndrome Failure to Thrive Ectodermal Dysplasia Abnormalities, Multiple Syndrome Chromosomes, Human, Pair 21 Prenatal Diagnosis Trisomy Maternal Age Metabolic Syndrome X Estriol Pregnancy Trimester, Second Pregnancy Amniocentesis Leukemia, Megakaryoblastic, Acute Fetal Diseases Chromosomes, Human, 21-22 and Y Nephrotic Syndrome Abortion, Eugenic Sjogren's Syndrome Intellectual Disability Infant, Newborn Turner Syndrome Karyotyping alpha-Fetoproteins Nasal Bone Nuchal Translucency Measurement Nondisjunction, Genetic Ultrasonography, Prenatal Pregnancy, High-Risk Pregnancy Trimester, First Williams Syndrome Myelodysplastic Syndromes Pregnancy-Associated Plasma Protein-A Chorionic Gonadotropin, beta Subunit, Human Cushing Syndrome False Positive Reactions Heart Defects, Congenital Disease Models, Animal Phenotype Paternal Age Acute Coronary Syndrome Polycystic Ovary Syndrome Chromosome Disorders Case-Control Studies DiGeorge Syndrome Horner Syndrome Craniofacial Abnormalities Prader-Willi Syndrome Long QT Syndrome Stanford-Binet Test Heart Septal Defects Risk Factors Guillain-Barre Syndrome Hemolytic-Uremic Syndrome Alzheimer Disease Duodenal Obstruction Mutation Genetic Testing Compartment Syndromes GATA1 Transcription Factor Tourette Syndrome Biological Markers Chorionic Gonadotropin Retrospective Studies Antiphospholipid Syndrome Pedigree Mosaicism Gestational Age Brain Porcine Reproductive and Respiratory Syndrome Klinefelter Syndrome Prevalence Neck

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