SMS Condition Report fast and easy

Simple instructions on how to SMS Condition Report

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Choose a document you want to add from the computer or integrated cloud storage service (Box, Google Drive, or OneDrive).
Access DocHub advanced editing tools with a user-friendly interface and change Condition Report in accordance with your needs.
SMS Condition Report and save changes.
Very easily fix any mistakes prior to going forward with the record export.
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How to SMS Condition Report

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What is SMS medical condition?

Smith-Magenis syndrome is a developmental disorder that affects many parts of the body. The major features of this condition include mild to moderate intellectual disability, delayed speech and language skills, distinctive facial features, sleep disturbances, and behavioral problems.

What are the behavior problems of Smith-Magenis syndrome?

Among self-injurious behaviors, fingers and hand biting are very evocative of SMS, especially in a child with development delay and sleep disorders. Aggressiveness directed toward others can also be seen. SMS children often seek for adult attention and seem to have low interest in other children [45, 51].

What is the life expectancy of someone with Smith-Magenis syndrome?

What is the life expectancy of individuals with SMS? As it is a relatively new syndrome, there isnt a detailed knowledge of theaverage life expectancy. However it is known that there was an adult with SMS who lived until she was 88 years old, and there are several adults with SMS in their 40s and 50s.

What is Smith-Magenis syndrome fact sheet?

Characteristics. Individuals with Smith-Magenis Syndrome are characterised by a short flat head, prominent forehead, broad square face, deep-set eyes, underdeveloped midface, broad nasal bridge, short nose, tented upper lip, and a chin that is small in infancy and becomes relatively prominent with age.

What are the symptoms of SMS syndrome?

What are the symptoms of Smith-Magenis syndrome? Abnormal cognitive development (intellectual disability). Short stature. Scoliosis. Limited sensation of pain or temperature. Raspy or hoarse voice. Hearing and/or vision problems. Excessive weight gain.

What is Smith-Magenis syndrome in children?

Smith-Magenis syndrome is a developmental condition caused by a chromosome deletion. The condition affects your childs ability to fall asleep and stay asleep, their ability to learn and their behavior. Theres no cure for Smith-Magenis syndrome, but treatment is supportive of symptoms that affect your child.

What are the physical characteristics of Smith-Magenis syndrome?

Characteristics. Individuals with Smith-Magenis Syndrome are characterised by a short flat head, prominent forehead, broad square face, deep-set eyes, underdeveloped midface, broad nasal bridge, short nose, tented upper lip, and a chin that is small in infancy and becomes relatively prominent with age.

What is the life expectancy of a child with SMS?

What is the life expectancy of individuals with SMS? As it is a relatively new syndrome, there isnt a detailed knowledge of theaverage life expectancy. However it is known that there was an adult with SMS who lived until she was 88 years old, and there are several adults with SMS in their 40s and 50s.

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