All individuals with variants in gene MRPS22

5 entries on 1 page. Showing entries 1 - 5.
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00095093 - - - - no - - - - - - COXPD5 Agenesis of corpus callosum, Hypertrophic cardiomyopathy, Pulmonary hypoplasia, Low-set ears 2 1 Karen Stals
00164760 17873122-Fam PubMed: Saada 2007 2-generation family, 3 affected sisters, unaffected carrier parents (first cousins) F yes Israel - - - - - ? see paper; ..., antenatal skin oedema, hypotonia, cardiomyopathy, tubulopathy 1 3 Johan den Dunnen
00164761 21189481-Pat PubMed: Smits 2011 2-generation family, 1 affected, unaffected carrier parents (first-grade relatives) M yes Pakistan - - - - - ? see paper; ..., Cornelia de Lange-like dysmorphic features, brain abnormalities, hypertrophic cardiomyopathy 1 1 Johan den Dunnen
00164762 25663021-Pat PubMed: Baertling 2015 2-generation family, 1 affected, unaffected carrier parents (first-grade consanguineous) M yes Turkey - - - - - ? see paper; ..., fatal neonatal lactic acidosis, brain and heart abnormalities 1 1 Johan den Dunnen
00301407 - - - ? - (Germany) - - - - - ? Strabismus (HP:0000486); Abnormality of the optic nerve (HP:0000587); Ataxia (HP:0001251); Global developmental delay (HP:0001263); Failure to thrive (HP:0001508); Lower limb spasticity (HP:0002061); Intention tremor (HP:0002080); Limb dystonia (HP:0002451); Increased CSF lactate (HP:0002490); Bilateral basal ganglia lesions (HP:0007146); Feeding difficulties (HP:0011968) 1 1 IMGAG
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