1p36 deletion syndrome

1p36 deletion syndrome is a chromosomal anomaly characterized by distinctive facial dysmorphic features, hypotonia, developmental delay, intellectual disability, seizures, heart defects, hearing impairment and prenatal onset growth deficiency.

Apnea

Lack of breathing with no movement of the respiratory muscles and no exchange of air in the lungs. This term refers to a disposition to have recurrent episodes of apnea rather than to a single event.


Total: 3

                       


(per page)
PMID (PMCID)
22425009
 MIXED_SAMPLE Child
Multiple causes of apnea in 1p36 deletion syndrome include seizures.
Kanabar G, Boyd S, Schugal A, Bhate S.
Seizure. 2012;21(5):402-6.
Multiple causes of apnea in 1p36 deletion syndrome include seizures.
22425009
 MIXED_SAMPLE Child
Multiple causes of apnea in 1p36 deletion syndrome include seizures.
Kanabar G, Boyd S, Schugal A, Bhate S.
Seizure. 2012;21(5):402-6.
Epileptic apnea is a feature of 1p36 deletion syndrome, though episodic apnea is multifactorial in these children, and may need repeated re-appraisal.
22425009
 MIXED_SAMPLE Child
Multiple causes of apnea in 1p36 deletion syndrome include seizures.
Kanabar G, Boyd S, Schugal A, Bhate S.
Seizure. 2012;21(5):402-6.
Epileptic apnea is a feature of 1p36 deletion syndrome, though episodic apnea is multifactorial in these children, and may need repeated re-appraisal.