All individuals with variants in gene MEGF10

11 entries on 1 page. Showing entries 1 - 11.
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00050575 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? intellectual disability, seizures 1 1 Johan den Dunnen
00155229 29311637-Fam3 PubMed: Saeed 2018 3-generation family, 2 affected (F, M), unaffected heterozygous carrier parents/relatives F;M yes Pakistan - - - - - obesity severe, early-onset obesity 1 1 Johan den Dunnen
00293711 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293712 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00293713 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00293714 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 141 Mohammed Faruq
00305005 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00361993 Pat14 PubMed: Saat 2021 - M yes Turkey - - - - - MYOP Hypotonia HP:0001252 1 1 Ibrahim Sahin
00408085 14 PubMed: Alabdullatif 2017 - F yes United Arab Emirates - - - - - retinal disease 20 months old female child born at term with prenatal course complicated by polyhydramnios. At birth she was found to have hypotonia, respiratory distress, feeding difficulty, and distal arthrogryposis (camptodactyly and overlapping toes). Respiratory distress progressed and she required invasive ventilation at the age of 4 months, then tracheostomy was placed at the age of 5 months and she had been dependent on ventilator since then. Gastrostomy tube was placed at that age as well. She also had developmental delay and echocardiogram showed patent ductus arteriosus and patent foramen ovale. Her physical examination showed weakness, hypotonia, areflexia, camptodactyly, overlapping toes, normal growth parameters, and distinctive facial features (dolichocephalic, broad nasal bridge, high arched palate, long smooth philtrum, and retrognathia). Electromyogram and nerve conduction studies were consistent with a myopathy. Her parents were second cousin and she had 3 older siblings. 1 1 LOVD
00442674 Pat46 PubMed: Westra 2019 - F - - - - - - - NMD deceased; severe hypotonia (most pronounces axial and proximal) with minimal facial expression and respiratory failure; muscle biopsy: increase in fiber size variation and presence of internal nuclei; EMG: myopathic changes with myotonic discharges; CK = 64 U/l 2 1 Johan den Dunnen
00442709 Pat81 PubMed: Westra 2019 - M - - - - - - - NMD - 1 1 Johan den Dunnen
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