How disabilities come to be Causes, roots, and beginnings

Reason 1. Its Genetic!DNA (deoxyribonucleic acid) is a nucleic acid that is the most basic unit of genetic information. Chromosomes are highly organized structures containing DNA in long strands. Most cells in our body (except for mature red blood cells) contain a complete set of 46 chromosomes, or 23 pairs.

Chromosomes, etc.The chromosomes are numbered 1-22 (largest to smallest) and the 23rd pair are the sex chromosomes, which determine our gender (two "X" chromosomes = female; one "X" and one "Y" chromosome = male). We inherit our chromosomes at the time of conception: one set of 23 from our mother and one set of 23 from our father. As we grow from a single cell into a complex human being, our chromosomes are copied into each new cell. < A>

GenesGenes are specific subunits or groups of DNA along thechromosomes. Just as our chromosomes come in pairs, so do our genes. Each gene codes for a protein (or chemical) that has a specific function in the body.

MeiosisMeiosis theformation of ova and sperm. During In this process, chromosomal mutations may occur.

Reason 1a. Autosomal dominant inheritance.Autosomal dominant conditions affect males and females equally, and only one gene of the pair needs to be abnormal for the individual to have the condition. Every child of an individual with an autosomal dominant condition has a 50% chance of inheriting the mutation and having the disorder.

Autosomal dominantIf the AD gene is there, it is expressed. No carriers here.Children have a 50/50 chance of also being affected by the disorder (one parent affected).

BOTH parents have dominant gene: Statistically, there is a 25% chance that the child will inherit the two unaffected genes and will be unaffected. There is a 50% chance that the child will inherit at least one affected gene, and will have the disorder.There is a 25% chance that the child will inherit both dominant genes, which is usually fatal.

Examples of AD NeurofibromatosisTuberous SclerosisMarfan SyndromeAchondroplasia**Osteogenesis Imperfecta (there are 7 distinct types; Type II is NM)Noonan syndrome**Cornelia de Lange syndrome**Apert syndrome**Treacher-Collins syndromeAniridia****new mutations originally; AD inheritance when passed from an affected individual.

Reason 1b. Autosomal recessive inheritance.Autosomal recessive conditions affect males and females equally, but both copies of the recessive gene have to be presentfor the individual to have the condition. Autosomal recessive conditions can be passed on when each parent is a "carrier" for the condition, and their offspring have a 25% risk of inheriting the condition. "Carriers" have one abnormal copy of the gene but do not have clinical symptoms and are not at increased risk to develop the condition. A family history of a recessive condition can reveal multiple individuals in a single generation (brothers and sisters) with the condition; in the case of small families, however, there may be only one affected individual.

Autosomal recessiveTwo carrier parents, statistically 1 unaffected, 2 carriers, and one affected. (25% chance of being affected by the recessive gene)

Autosomal recessive one carrier parent As indicated, if only ONE parent is a carrier of a recessive trait, then there is no chance for one of the children to be affected; however, a 50% chance of being a carrier.

Autosomal recessive one affected parent; one non-carrier:All children will be carriers, since theymust inherit one affected (recessive) gene from the affected parent, but one (dominant) gene from theunaffected parent.

Autosomal recessive: one affected parent; one carrier parent:With the carrier parent, the statistics change to a 50% chance of being affected; 50% chance of being a carrier.

Examples of AR Usher syndromeRetinitis pigmentosa (AR in 20% to 25% of cases; AD in 15% -- 20%; XLR in 10% -- 15%)Tay-Sachs diseaseSickle Cell AnemiaPhenylketonuriaBatten diseasePendred syndromeSpinal Muscular AtrophyAlbinismTorsion Dystonia (or AD)

Reason 1c. X-Linked Recessive InheritanceMost X-linked conditions occur in males who inherit an abnormal copy of the gene from their mothers. Since males only have one X chromosome, if it carries an abnormal copy of the gene, they will suffer from the disorder. These mothers carry a copy of the altered gene but are usually unaffected if their other X chromosome has a normal working copy of the gene.

X-Linked RecessiveAn affected male never transmits the disease to his sons since the X chromosome is always passed on from mother to son. When the mother carries a copy of a gene for an X-linked disease, the chance of inheriting the altered gene is 1 in 2 in each pregnancy for both boys and girls, but only the male offspring will be affected.

X-linked recessive: affected father:In this family, the father is affected by an X-linked (recessive) disorder. The sons inherit the Y chromosome from their father. All daughters inherit a recessive gene, i.e., are healthy carriers.

X-linked recessive: carrier mother; affected father:If the mother is a carrier (XXa) and the father is affected (XaY), the children will statistically be: (girls: 50% carrier, 50% affected; boys: 50% unaffected; 50% affected) Mother: X XaFather: XaY XXa(carrier girl)XaXa(affected girl)XY (unaffected boy)XaY (affected boy)

X-linked recessive: affected mother (XaXa) and father (XaY)Mother and father are affected by the X-linked recessive gene: all children are affected by the recessive gene.MotherXaXa

Father Xa

YXaXa (affected girl)XaXa (affected girl)XaY(affected boy)

XaY (affected boy)

Examples of XLR Color BlindnessHemophiliaFragile X SyndromeDuchenne Muscular DystrophySpinal Bulbar Muscular atrophyNorrie DiseaseMenkes syndrome

Reason 1d: X-linked Dominant InheritanceWhen an X-linked gene is said to express dominant inheritance, it means that asingle dose of the mutant allele will affect the phenotype of the female. A recessive X-linked gene requires two doses of the mutant allele to affect the female phenotype. The following are the hallmarks of X-linked dominant inheritance: ~The trait is never passed from father to son.~All daughters of an affected male and a normal female are affected. All sons of an affected male and a normal female are normal.~Matings of affected females and normal males produce 1/2 the sons affected and 1/2 the daughters affected.~Males are usually more severely affected than females. The trait may be lethal in males.~In the general population, females are more likely to be affected than males, even if the disease is not lethal in males.

X-linked dominantOffspring of either gender have a 50/50 chance of inheriting XLD, if the mother is affected. If the father is affected, the boys will not be affected, but girls will always.

Examples of XLD Aicardi syndrome (occasional new mutation)Charcot-Marie Tooth Disease (type X)Hypophosphatemic ricketsRett syndrome

Reason 1e: Sporadic or new mutationsA MUTATION is a sudden, permanent change in DNA.This change has the potential to cause disorders or diseases.A sporadic or new mutation of this sort has no real risk for recurrence, as a general rule, and remember rules are always broken.

Examples of Sporadic/New mutation Trisomy 13 (Patau syndrome)Trisomy 18 (Edwards syndrome)Trisomy 21 (Down syndrome)Cri-du-chat syndromePrader-Willi syndromeRubenstein-Taybi syndrome

Here are some syndromes that belong in this category but could be considered in the X-linked. But they go here, OK?XXY syndrome (Klinefelter syndrome)XXX syndromeTurner syndrome (XO)XYY syndromeAnd other disorders involving multiple Xs or Ys.

Reason 2: MultifactorialMany reasons exist that might actually cause these disorders some genetic, some environmental, some because of the interplay between the genes and environment. So all of those disorders go HERE.

Examples of multifactorial:Spina BifidaCancerCleft palateOsteoporosisMeningitisCongenital heart defectsEncephalitisAnencephalyMicrocephalyPyloric StenosisHydrocephaly

Reason 3: Perinatal incidentsConditions, complications, incidents, accidents, mistakes, the unfolding of unfortunate events that occur before, during, or immediately following childbirth.

Examples of Perinatal JaundiceCerebral palsyPrematurityRespiratory distress syndromeFailure to thrive (maybe )Anoxia

Reason 4a: TeratogensAgents that cause malformations in a developing embryo. These agents cross the placental barrier and cause or increase the incidence of physical malformations and behavioral and cognitive deficits. Examples are any medication, chemical, infectious disease, or environmental agent that might interfere with the normal development of a fetus; result in the loss of a pregnancy, a birth defect, or a pregnancy complication.

Examples of teratogens ToxoplasmosisFetal Alcohol SyndromeCocaine-exposed or addicted

Reason 4b: Maternal conditionsInfections, diseases, or disorders of a mother during pregnancy, sometimes having the potential to injure the unborn child.

Examples of Maternal condition:AIDSHIVHerpesCongenital rubella syndromeCytomegalovirus

Reason 5: AbuseThe physical or mental injury, sexual abuse, or negligent treatment of a child under the age of 18 by a person who is responsible for the child's welfare. The specific types are physical abuse, physical neglect, emotional abuse, emotional neglect, sexual abuse, sexual exploitation, physical endangerment, abandonment, medical and psychological neglect, educational neglect, and improper ethical guidance.

Examples of Abuse Shaken Baby SyndromeNonorganic Failure to Thrive

REASON 6: Accident, Injury, IllnessMany disabilities with long-term consequences are caused by accidents or illness. Some disabilities are directly the result of the accident or illness; others as a secondary condition.

Reason 7: UnknownNo idea. Well, maybe an idea, but nothing has panned out so far. But still looking. Well let you know.

Examples of UNKNOWN AutismAmblyopiaSudden Infant Death SyndromeAsperger SyndromeDyslexiaADHDEpilepsyScoliosis Celiac Disease

*Retinitis pigmentosa AR in 20% to 25% of cases, AD in 15% -- 20%; XLR in 10% to 15%***