SMS Child Medical History fast and easy

Easy guide on the way to SMS Child Medical History

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How to SMS Child Medical History

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In this video tutorial, Dr. Emma checks in with a patient named Celia regarding her diabetes management. They discuss Celia's current situation, including the use of a pump for blood sugar control. Celia reports that her blood sugar levels have mostly been stable, with only occasional highs. The conversation touches upon Celia's diagnosis at the age of six, assisted by her mother’s input. Dr. Emma plans to ask a few questions to better understand Celia's health status and will take notes during the chat to potentially create a plan for any necessary actions.

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What is the diagnosis Smith-Magenis syndrome?

Clinical characteristics. Smith-Magenis syndrome (SMS) is characterized by distinctive physical features (particularly coarse facial features that progress with age), developmental delay, cognitive impairment, behavioral abnormalities, sleep disturbance, and childhood-onset abdominal obesity.

What are symptoms of SMS?

Common symptoms include: 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 the treatment for SMS?

Two treatment modalities will be evaluated alone and in combination: 1) light-induced suppression of daytime melatonin release and delay of nighttime sleep; and 2) pharmacological replacement of nocturnal melatonin.

What is the prognosis for Smith-Magenis syndrome?

The prognosis for Smith-Magenis syndrome is dependent on the severity of your childs symptoms. Some people diagnosed with the condition have a normal life span and can live semi-independently with limited support from their family, friends and caregivers.

What does SMS mean in medical terms?

Smith-Magenis syndrome (SMS) is a complex developmental disorder that affects multiple organ systems of the body. The disorder is characterized by a pattern of abnormalities that are present at birth (congenital) as well as behavioral and cognitive problems.

What is SMS life expectancy?

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.

How is Smith-Magenis syndrome inherited?

Inheritance. Smith-Magenis syndrome is usually not inherited. This condition typically results from a chromosomal deletion or an RAI1 gene variant that occurs during the formation of reproductive cells (eggs or sperm) or in early fetal development.

Is SMS a form of autism?

Individuals with Smith-Magenis syndrome often receive diagnoses of Autism Spectrum Disorder (ASD) and high rates of autism have been reported; however, due to differences in methods used by studies, the reported rates of ASD range between 50-93%.

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SMS Child Medical History