Disease #05170 (IE (encephalopathy, infantile (IE)))

Official abbreviation IE
Name encephalopathy, infantile (IE)
OMIM ID -
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2016-05-26 16:15:47 +02:00 (CEST)
Date last edited N/A


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00065256 26708753 F1_IV:5 PubMed: Shamseldin HE 2016, Journal: Shamseldin HE 2016 - M yes Saudi Arabia - >06y06m - - - IE Autosomal-Recessive Severe Infantile Encephalopathy; cachexia (HP:0004326), severe muscular hypotonia (HP:0001252), microcephaly (HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) UNC80 UNC80 1 1 Pieter Klap
00065257 26708753 F2_IV:1 PubMed: Shamseldin HE 2016, Journal: Shamseldin HE 2016 - M yes Saudi Arabia - >02y - - - IE Autosomal-Recessive Severe Infantile Encephalopathy; cachexia (HP:0004326), severe muscular hypotonia (HP:0001252), Microcephaly (HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) UNC80 UNC80 1 1 Pieter Klap
00065258 26708753 F2_IV:2 PubMed: Shamseldin HE 2016, Journal: Shamseldin HE 2016 - M yes Saudi Arabia - >01y - - - IE Autosomal-Recessive Severe Infantile Encephalopathy; Cachexia (HP:0004326), severe muscular hypotonia (HP:0001252), no microcephaly (-HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) UNC80 UNC80 1 1 Pieter Klap
00065259 26708753 F3_IV:4 PubMed: Shamseldin HE 2016, Journal: Shamseldin HE 2016 - F yes Saudi Arabia - >07y - - - IE Autosomal-Recessive Severe Infantile Encephalopathy; Cachexia (HP:0004326), progressive muscular hypotonia (HP:0001252), Microcephaly (HP:0000252), no seizures (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) UNC80 UNC80 1 1 Pieter Klap
00065260 26708753 F4_V:1 PubMed: Shamseldin HE 2016, Journal: Shamseldin HE 2016 - F yes Egypt - >08y - - - IE Autosomal-Recessive Severe Infantile Encephalopathy; borderline cachexia (HP:0004326), progressive muscular hypotonia (HP:0001252), no microcephaly (-HP:0000252), single seizure (HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) UNC80 UNC80 1 1 Pieter Klap
00065262 26708753 F4_V:2 PubMed: Shamseldin HE 2016, Journal: Shamseldin HE 2016 - F yes Egypt - >04y - - - IE Autosomal-Recessive Severe Infantile Encephalopathy; borderline cachexia (HP:0004326), progressive muscular hypotonia (HP:0001252), no microcephaly (-HP:0000252), no seizure (-HP:0001250), minor abnormality of the face (HP:0000271), Global developmental delay (HP:0001263) UNC80 UNC80 1 1 Pieter Klap
00207359 - - - - no - - - - - - IE fatal infantile encephalopathy SCO1 SCO1 2 1 Eric Shoubridge
00207498 ZY07 PubMed: Lin et al., 2018 First family with PIGA-associated epileptic encephalopathy in Taiwan. Proband is third child of a pair of nonconsanguineous healthy parents. M no Taiwan Taiwanese >00y03m - - Anti-epileptic drugs, levodopa IE Systemic cyanosis and muscular hypotonia. Facial dysmorphism (depressed nasal bridge, large mouth, high-arched palate, micrognathia). Severe global DD, axial hypotonia and dyskinasia. Epileptic spasms and erratic myoclonic seizures. Progressive brain atrophy, delayed myelination, thin corpus callosum. Bilateral hydronephrosis. Elevated ALP level (405 IU/L) PIGA PIGA 1 1 Philippe Campeau
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