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Clinical Genetics
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Conditions Treated
Symptoms Commonly Seen
Treatments Commonly Offered
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Related questions

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Recent

A 34-year old asked:

Can genetic testing prevent birth defects in pregnancy?

1 doctor answer • 2 doctors weighed in

A 21-year old asked:

How can I know if I have iron overload/hemochromatosis? What tests should be performed? I hear that there is a DNA genetic test kit for hemochromatosis, is that true?

1 doctor answer • 1 doctor weighed in

A 41-year old asked:

How did our ancestors on the prairie treat Duchenne muscular dystrophy?

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A 32-year old asked:

What are the treatments available for duchenne muscular dystrophy?

2 doctor answers • 2 doctors weighed in

A 30-year old female asked:

pediatrian has concerns about my sons facial features he has a smooth philtrum a long head and small ears sending him for genetic testing why is this?

3 doctor answers • 14 doctors weighed in

A 36-year old asked:

Could a white forelock be a sign of waardenburg syndrome?

3 doctor answers • 12 doctors weighed in

A 25-year old asked:

Can you have genetic counseling for any psychiatric diseases?

2 doctor answers • 7 doctors weighed in

A 44-year old asked:

Are there any proven effective treatments for neurofibromatosis?

1 doctor answer • 2 doctors weighed in

A 21-year old asked:

What is the difference between neurofibromatosis1 and neurofibromatosis 2?

1 doctor answer • 3 doctors weighed in

A 42-year old asked:

Can neurofibromatosis kill you?

2 doctor answers • 2 doctors weighed in

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Conditions Treated

Congenital abnormalities
Uterine abnormalities
Bleeding disorders
Birth defects
Cartilage disorders
Down syndrome
Dyslexia
Multiple sclerosis (MS)
Polycystic kidney disease
Thalassemia
Iron overload (hemochromatosis)
Hemophilia
Leukodystrophy
Anencephaly
Inherited metabolic disorders
Charcot marie tooth
Fabry disease
Maple syrup urine disease
Mucopolysaccharidoses
Factor VIII deficiency
Chromosomal abnormalities
Hereditary colon cancer
Von recklinghausen's disease
Mucolipidoses
Tay-sachs disease
Christmas disease
Hemolytic disease of newborn
Usher syndrome
Hereditary ovarian cancer
Mitochondrial disorder
Chronic granulomatous disease
Klinefelter's syndrome
Double outlet right ventricle
Chronic myelogenous leukemia
Angelman syndrome
Neurofibromatosis
Severe combined immunodeficiency
Marfan syndrome
Niemann pick disease
Hereditary breast cancer
Prader-willi syndrome
Patau syndrome (trisomy 13)
Esophageal atresia
Edwards syndrome
Von hippel lindau disease
Wiskott aldrich
Werner syndrome
Ehler-danlos syndrome
Inherited metabolic disorders in fetus
Congenital adrenal hyperplasia
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Symptoms Commonly Seen

Photosensitivity rash
Scalp defect

Treatments Commonly Offered

Salt water rinse
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