Laron syndrome (patient information)
For the WikiDoc page for this topic, click here
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Jinhui Wu, MD
Please Join in Editing This Page and Apply to be an Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [2] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
What is Laron syndrome?
How do I know if I have Laron syndrome and what are the symptoms of Laron syndrome?
The principal feature of Laron syndrome is abnormally short stature
- Short hands and short feet
- Unusual facies: Prominent forehead, deep-set eyes, blue sclera, saddle nose and depressed nose bridge
- Proportionally larger head and abnormal skull growth
- High-pitched voice
- Reduced or normal intelligence
- Delayed bone age
- Delayed menstruation onset in girls
- Small penis in boys
- Delayed sexual development
- Childlike proportions in adults
- Obesity
Who is at risk for Laron syndrome?
How to know you have Laron syndrome?
When to seek urgent medical care?
Treatment options
Diseases with similar symptoms
- Intrauterine growth retardation
- Constitutional delay of growth
- Idiopathic short stature
- Nutritional growth retardation
- Psychosocial short stature
Where to find medical care for Laron syndrome?
Directions to Hospitals Treating Laron syndrome
Prevention of Laron syndrome
What to expect (Outook/Prognosis)?
Copyleft Sources
http://emedicine.medscape.com/article/922902-overview