Pallister-Killian syndrome

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What is Pallister-Killian syndrome?

Pallister Killian mosaic syndrome is genetic condition. It is characterized by weak muscle tone (hypotonia), intellectual disability, developmental delay, distinctive facial features, seizures, areas of unusual skin coloring (pigmentation), and other birth defects.

Common symptoms reported by people with Pallister-Killian syndrome

Common symptoms
How bad it is
What people are taking for it

Reports may be affected by other conditions and/or medication side effects. We ask about general symptoms (anxious mood, depressed mood, fatigue, pain, and stress) regardless of condition.
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Treatments taken by people with Pallister-Killian syndrome

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Compare treatments taken by people with Pallister-Killian syndrome

Let’s build this page together! When you share what it’s like to have Pallister-Killian syndrome through your profile, those stories and data appear here too.

Got a question about living with Pallister-Killian syndrome? Members in the forum might have the answers.

Who has Pallister-Killian syndrome on PatientsLikeMe?


Age
Age Proportion # of patients
<20 2
20s 1
30s 1
40s 0
50s 0
60s 0
70+ 0
Age at first symptom
Age at first symptom Proportion # of patients
0-19 years 2
20-29 years 1
30-39 years 0
40-49 years 0
50-59 years 0
60-69 years 0
70+ years 0

Distribution of sex

Sex
Sex Proportion # of patients
Male 3
Female 1

Diagnosis status
Diagnosis status Proportion # of patients
Diagnosed 4
Not Diagnosed 0

These charts show data from Pallister-Killian syndrome patients who have completed their condition history
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Let’s build this page together! When you share what it’s like to have Pallister-Killian syndrome through your profile, those stories and data appear here too.

Got a question about living with Pallister-Killian syndrome? Members in the forum might have the answers.