Genetics Disorders

Hemophilia is the ability of the blood clot evenly reduced causing sufferer to bleed severely.The Average age of diagnosis is 2 to 3 years old. Test used to detect when blood has low levels of any clotting. Located on Chromosome X. Hemophilia is Sex-Linked. Symptoms of diseases are nose bleeds,Bruising,and Blood in Urine.

Hemophilia

Tay Sachs is a life threatening disease often in nervous system passed down through your family. Average age of diagnosis 4 or 5 years of age. Carrier test used to detect. Tay Sachs is located on chromosomes 15. Tay Sachs is sex-link. Symptoms of Disease muscle weakness, and low muscle tone.

Tay Sachs

Sickle Cells

Sickle Cell the Red Blood Cells  which one normally shaped liked a disc take on a sickle crescent shape. Average of Diagnosis is 4 months. Test used to detect is Blood Test. Located on the 11 Chromosome. Sickle Cell is Autosomal. Symptoms of Disease are Hand foot syndrome Delayed growth and frequent infections.

Muscular Dystrophy is a group Inherited disorders that involve muscle weakness and loss of muscle tone. Average age of Diagnosis is around 4 years of age. Test used to detect is a physical exam. Located on the X chromosome. Muscular Dystrophy is sex-linked. Symptoms of Disease are frequent falls, waddling gait, large calf muscles.

Colorblindness is a inability to see certain colors in the usual way. Average age of Diagnosis is 5 years of age. Test used to detect are color exam. Located on the X chromosome. Color Blindness is Sex-Linked. Symptoms of disease are rapid eye movement difficulty distinguishing between colors

Parkinsons is a disorder of the brain that leads to shaking  and difficulty with walking and movement coordination.  Avwerage age of diagnosis 60 years of age. No test to detect The disease. Located on the 4 and 6  Chromosome.  Parkinsons is Autosomal. Symptoms for disease slowed movement Rigid Movement.

PKU is a baby born without the ability to properly break down amino acid. Average age Diagnosis is 3 weeks  Test used to determine Pku test. Located on the 12 Chromosome. PKU is Autosomal. Symptoms for disease lose in interest in their surroundings.

Huntington Disease is a disorder passed through families in which bad nerve cells. Average of Diagnosis 61 years old. Test used to determine is Neurological examination. Located on the 4 chromosome. Symptoms for Disease Mmovement disorders and cognitive Disorders. Huntington Disease is autosomal.

Dwarfisim is an unusually or ab normally low stature or small size. Average age of Diagnosis Birth. Test used to detect measurements.  Located on the 4 chromosome. Dwarfism is located on 4 chromosome. Dwarfism is Sex linked. Symptoms shortness in stature.

Down Syndrome is Genetic condition in which a person has 47 chromosomes instead of 46. Average age of Diagnosis At birth. Test used to detect diagnostic Test. Located on the 21 chromosome. Down Syndrome is Sex-Linked. Down Syndrome flattened facial features upward slanted ears.

Cystic Fibrosis is passed down by family that causes thick, sticky mucous to build up in the lungz. Average age of diagnosis is at birth. Test used to detect is Screening. Located on the 7 chromosome. Cystic Fibrosis is Autosomal. Symptoms of disease is Coughing and weezing.

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