All individuals with variants in gene PLCB3

2 entries on 1 page. Showing entries 1 - 2.
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00207812 29122926-Fam PubMed: Ben-Salem 2018 4-generation family, 2 affected cousins, unaffected heterozygous carrier parents M yes United Arab Emirates - - - - - ? postnatal growth deficiency, profound limb shortening with proximal and distal segments involvement, narrow chest, radiological abnormalities involving spine, pelvis and metaphyses, corneal clouding and intellectual disability 1 2 Johan den Dunnen
00385552 Fam2Pat4 PubMed: Ritelli 2018 - F - Italy - - - - - CHTD facial dysmorphism; hearing loss/recurrent otitis; heart anomalies; mitral valve dystrophy/insufficiency; tricuspid valve dystrophy/insufficiency.; aortic valve dystrophy/insufficiency; atrial septum aneurysm; arrhythmias; other soft connective tissues; abnormal skin texture; joint hypermobility; habitus/orthopedics; short stature; short limbs; neurinoma; palmoplantar keratoderma 1 1 Johan den Dunnen
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