Disease #03404 (DEE11 (encephalopathy, developmental and epileptic, type 11), OMIM:613721)

Official abbreviation DEE11
Name encephalopathy, developmental and epileptic, type 11
OMIM ID 613721
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene SCN2A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2022-04-07 09:19:02 +02:00 (CEST)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00081086 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - DEE11 Epileptic encephalopathy, early infantile, 11 (OMIM:613721) SCN2A SCN2A 1 1 Daniel Trujillano
00380939 185035 - - M no Germany - - - - - DEE11 Bilateral tonic-clonic seizure, Neonatal seizure, Neonatal epileptic spasm SCN2A SCN2A 1 1 Andreas Laner
00416926 1578 PubMed: Tzialla 2022 - M no (Italy) Caucasian - - - - DEE11 Macrocephaly HP:0000256 Ventriculomegaly HP:0002119 Supraventricular tachycardia HP:0004755 Cardiomegaly HP:0001640 Decreased body weight HP:0004325 Simplified gyral pattern HP:0009879 Low-set ears HP:0000369 Blepharophimosis HP:0000581 Epicanthus HP:0000286 Hypertelorism HP:0000316 Retrognathia HP:0000278 Hypotonia HP:0001252 Seizure HP:0001250 Fever HP:0001945 Hyponatremia HP:0002902 Hypoglycemia HP:0001943 Anemia HP:0001903 SCN2A SCN2A 1 1 Edoardo Errichiello
00424614 159736 - - F ? - - - - - - DEE11 Dystonia, Intellectual disability, mild, Ventricular septal defect, Lower limb spasticity, Aganglionosis of the small intestine, Arm dystonia SCN2A SCN2A 1 1 Andreas Laner
00428060 208447 - - M no Germany - - - - - DEE11 Focal tonic seizure, Neurodevelopmental delay SCN2A SCN2A 1 1 Andreas Laner
00436412 269208 - - M no Germany - - - - - DEE11 Severe global developmental delay, Microcephaly, Hypertelorism, Long palpebral fissure SCN2A SCN2A 1 1 Andreas Laner
00465814 331736 - - F - Germany - - - - - DEE11 Neurodevelopmental delay, Motor delay, Gait ataxia, Absent speech, EEG abnormality, Neurodegeneration SCN2A SCN2A 1 1 Andreas Laner
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