Syndromes and Birth Defects

Slides:



Advertisements
Similar presentations
Down Syndrome Training The Center for Life Enrichment
Advertisements

Birth Defects.
4/14/2017 PKS Kids A non-profit organization for those affected by Pallister-Killian Syndrome
Basic Facts on Birth Defects
Genetic Diseases.
Turner’s Syndrome An Original Presentation from Mrs
TURNER sYNDROME By: Jazmin Barnes.
Nondisjunction Homework for 11/13/14
genetics. utah. edu/units/disorders/whataregd/down/index
Down syndrome.
By: Whinter Kent and Bobbi McKennie
Trisomy 21 Down Syndrome Marissa Lazenby Comm 1010.
BIRTH DEFECTS. CEREBRAL PALSY The term cerebral palsy refers to any one of a number of neurological disorders that appear in infancy or early childhood.
Genetic Disorders Problem Pregnancies.
Nicolette Laird Period 3
Shelby Herstine, Fillie Landi, Mike LeBus
PRENATAL INTRO & BIRTH DEFECTS AFTER CONCEPTION…..
Human Genetic disorders
Trisomy 21 (Down’s syndrome)
Genetic Disorders.
Presentation By: Katherine Mateos
CHARGE Syndrome By: Kylie LeHew Whitney Webb. What does CHARGE stand for? C stands for Coloboma of eye (parts of eyes don’t develop). H stands for heart.
Fragile X Syndrome Priya Sankaran.
- When DNA Mutates. MUTATION A heritable change in the nucleotide sequence of an organism’s DNA.
Interesting Genetic Disorders and Diseases, and Abnormalities.
Birth Defects Taryn Ballmann. Cleft Lip & Cleft Palate O The tissue that forms the lips or roof of the mouth do not join completely before birth O Can.
Birth Defects Taryn Ballmann.
Numerical Chromosomal disorders
Genetic Disorders and Birth Defects. Cleft lip/pallet Affects: anyone, more common in asians and native americans When appears: birth Method of inheritance:
27.3 Genetic Disorders Errors in the chromosome number
Sally Freese Family and Consumer Science
Ashley Osborne Quesha McClanahan Orchi Haghighi
Birth Defects By: Andrew and Sarah.
MMR Patient with special challenge Dr. Miada Mahmoud Rady.
Birth Defects. FACTS  About 150,000 babies are born each year with birth defects.  The parents of one out of every 28 babies receive the frightening.
 Definition Definition  Symptoms: Symptoms: › The Skeleton The Skeleton › The Eye The Eye › The Skin The Skin  Treatment Treatment  Genes Genes 
Chromosomal Karyotypes. Chromosomes Definition Genetic structures of cells containing DNA Identification Each chromosome has a characteristic length and.
Genetic Disorders, Part Deux
Marfan Syndrome Jenna Blythe.
Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display Forming a New Life: Conception, Heredity, and Environment.
Year 10 Science Health and disease
Chromosomal Aberrations Can be caused either by –non-disjunction (failure of whole chromosomes to separate during meiosis) –translocation (bits of chromosomes.
Genetic Counseling (Down Syndrome) From: Shelby Finnie.
Dwarfism By: Hannah Nugent.
Bone Disorders Honors Anatomy & Physiology Ms. Susan Chabot.
Picture from: By: Heather Williams.
Karyotyping.
Genetic Disorders What is a Genetic Disorder? Caused by abnormalities in an individual’s genetic material (the DNA, or the genome). There are four different.
Fetal Alcohol Effects.
Atypical Meiosis BC Science Probe 9 Section 4.5 Pages
Cri-du-chat Syndrome By: Maddy Gordon. What is Cri-du-chat syndrome? Cri-du-chat syndrome is a rare chromosomal condition that results when a piece of.
BIRTH DEFECTS Frank Zuniga.
A defect of the 21 st chromosome By: Nur Ajeerah Esah Binti Zainuddin Dietetic 3.
DOWN SYNDROME NUR HAMIZA RUZAINI BT HASHIM. WHAT IS DOWN SYNDROME Down syndrome is a genetic condition that causes delays in physical and intellectual.
Chromosomal Disorders (Syndromes) ************************
Down Syndrome Effects In some cases, certain Down syndrome effects, such as hypotonia, may be present at birth; others may not become evident until.
Down Syndrome Training The Center for Life Enrichment
Clinical features Down's syndrome is usually suspected at birth because of the baby's facial appearance.
MoeBius Syndrome.
Down Syndrome Vanessa Tam 12A.
Cleft Lip or Palate.
Karyotypes and Genetic Disorders
Human Genetics.
CAN YOU IDENTIFY THE DISEASE?
By: Monica Mendez Niah homyak
Presentation transcript:

Syndromes and Birth Defects Beth Rutter Help Me Grow Service Coordinator

What is a syndrome? Clinically recognizable features (observed by a physician) Symptoms reported by the patient Involves multiple body systems (cardiovascular, craniofacial, neurological, vision, hearing, etc.) Often named for the first diagnosed patient or the physician who discovered the disease

Most Common Syndromes Down Syndrome Marfan Syndrome Fragile X

Down Syndrome Affects 1 in 800 births Chromosomal abnormality due to additional copy of Chromosome 21 resulting in having 47 chromosomes instead of 46 Can affect the heart, gastrointestinal system, vision, hearing, thyroid and cause learning and developmental delays Diminished muscle tone Most recognizable syndrome due to facial features

Facial Features of Down Syndrome Eyes that slant upward Small ears that may fold over a little at the top A small mouth, making the tongue appear large A small nose with a flattened nasal bridge A short neck Small hands and feet Low muscle tone Short stature in childhood and adulthood

Children with Down Syndrome have special health needs Glasses and/or hearing aids Medication for thyroid levels Open heart surgery or medication for heart defects Specialized diet due to Hirschsprung’s Disease Colostomy bag due to Hirschsprung’s Special diet to ensure healthy weight

Developmental Characteristics of Children with Down Syndrome Delayed motor skills Including oral motor therapy for feeding/speech issues due to decreased muscle tone in jaw/mouth Delayed communication skills Delayed cognitive development

Marfan Syndrome 1 in 5,000 births Inherited connective tissue disorder Involves heart, blood, eyes, skeletal Tall and slender build Disproportionately long arms, legs, fingers and toes A breastbone that protrudes outward or dips inward A high, arched palate and crowded teeth Heart murmurs Extreme nearsightedness A curved spine Flat feet

Special Needs of Children with Marfan Syndrome Physical, occupational and speech therapy Medication for cardiovascular health Glasses Some physical limitations to ensure safety Cannot ride roller coasters Rough and tumble play might be limited Should avoid jump houses or trampolines

Developmental Characteristics of Children with Marfan Syndrome Delayed physical skills Delayed communication skills Delayed cognitive skills Development can be delayed due to multiple heart surgeries or illness

Fragile X More severe in males due to two X chromosomes Large /protruding ears Recurrent otitis media in childhood Soft skin Flexible joints ( particularly fingers, wrists, elbows) Low muscle tone Flat feet Long face Large testicles  (males) Seizure disorder Often dual diagnosis of mental retardation and or Autism

Developmental Characteristics of Children with Fragile X Delayed physical development Delayed communication Delayed cognitive development Delayed social development

Other Common Syndromes DiGeorge Syndrome: heart, craniofacial, palate, growth hormone deficiency, renal issues CHARGE Syndrome: coloboma, heart, atresea of the nasal choanae, retardation of growth, genital or urinary, ear abnormalities and deafness HELLP Syndrome: prenatal, hemolytic anemia, elevated liver enzymes, low platelet count Angelman Syndrome: neurological (seizures), vision (strabismus), hypopigmentation of hair and eyes

What is a birth defect? Birth defects are defined as abnormalities of structure, function, or body metabolism that are present at birth. These abnormalities lead to mental or physical disabilities or are fatal. There are more than 4,000 different known birth defects, ranging from minor to serious, and although many can be treated or cured, they're the leading cause of death in the first year of life. Caused by genetic, environmental or unknown factors.

Most Common Birth Defects Heart Lip Palate Limbs Neural Tube Defects

Congenital Heart Defects Any defect of the heart that is present at birth Atrial Septal Defect (ASD) Ventral Septal Defect (VSD) 1 in 125 babies are born with CHD Multiple causes and is often a characteristic of a syndrome but can stand alone ASD and VSD can be remedied with medication or surgery but can resolve without either, through growth

Lip and Palate Defects Cleft lip Cleft Palate Feeding is often difficult Dental development is affected Surgery can remedy clefts and often go unnoticed due to advances in plastic surgery Fetal development stalls causing an opening or “cleft” which doesn’t close Can be a sign of a syndrome such as Pierre-Robin

Limb Defects Amniotic Banding is most common. Theory is that the amniotic sac causes the banding after rupture Finger loss is most common with full limb loss secondary Clubfoot is also common in babies with amniotic banding

Neural Tube Defects Spina Bifida Midline Defects Neural tube development stops at a certain point on the spine, location of myelocele determines what control the child has over lower limbs, bowels and bladder Children usually have shunts to prevent accumulation of spinal fluid Cognitive development is usually typical, or advanced

Questions?