Specific
Characteristics
- · Autosomal dominant genetic disorder
- · Also known as multiple lentigines syndrome
- · Lentigines, dark brown string-like spots, cover the skin
Causes
- · Caused my mutations in the PTPN11 and RAEF1 genes.
- · 50% chance on an affected parent passing the disease on to her offspring.
Signs and Symptoms
- · Lentigines; numerous black or dark brown spots, in varying lengths and shapes, on the skin
- · Electrocardiographic conduction defects; irregular electric impulses from the heart. Severe cases can result in fainting episodes, seizures, etc.
- · Ocular hyperterlorism; anatomical malfunctions in the formation of the head and facial areas
- · Pulmonary stenosis
- · Abnormalities of the genitals. Males experience unusual acuteness of the penis and/or failure of one or both testes. Females will experience underdeveloped or even absent ovaries.
- · Retarded growth; stunt in bone growth and/or growing of a bone down the chest’s center.
Pulmonary Stenosis |
Diagnosis
- · Pale or tan discolorations of the skin at birth.
- · A parent or sibling has multiple lentigines.
- · X-ray and electrocardiography (EKG) exams will show internal birth defects in skeletal and electric impulses.
Treatment
- · Surgery, depending upon the location and severity of the affected areas.
- · Treatment, depending on the severity of the condition, not always necessary.
- · Hormone injections for affected individuals with abnormalities in genitals.
- · Hearing aids and speech therapy for affected individuals with damaged hearing.
References
Multiple
lentigines syndrome - Genetics Home Reference. (n.d.). Genetics Home
Reference - Your guide to understanding genetic conditions. Retrieved
September 13, 2013, from
http://ghr.nlm.nih.gov/condition/multiple-lentigines-syndrome
Pulmonic
Stenosis. (n.d.). Home. Retrieved September 13, 2013, from
http://www.marvistavet.com/html/pulmonic_stenosis.html
rare-diseases
— National Organization for Rare Disorders. (n.d.). Welcome to NORD —
National Organization for Rare Disorders. Retrieved September 13, 2013,
from
http://www.rarediseases.org/rare-disease-information/rare-diseases/byID/718/viewFullReport
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