All individuals with variants in gene LMNB2

4 entries on 1 page. Showing entries 1 - 4.
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AscendingIndividual ID     

ID_report     

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VIP     

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Owner     
00324284 LMNB2 patient - - F yes Iran - - - no none epilepsy HP:0002123 HP:0002123 HP:0002123 1 1 Ehsan Razmara
00449812 - - - M - - (not applicable) white - - - - microcephaly HP:0000253, HP:0000271, HP:0001363, HP:0001249 1 1 Marketa Wayhelova
00465222 FamPat1 PubMed: Desgrouas 2025 2-generation family, 2 affected sibs, unaffected heterozygous carrier parents - yes France - 00y00m01d - - - ? see paper; ..., 22wg-fetal growth retardation, severe microcephaly (−6ZS), ponto-cerebellar hypoplasia; birth 39wg, weight lower normal range (1860 g), 30 min-deceased; hypertrichosis, facial dysmorphism (low-set ears, hypertelorism, macrostomia, retromicrognathia; multiple joint contractures, restricted limb movements, lower limbs remained permanently in hyperextension; no fetal autopsy 1 2 Johan den Dunnen
00465223 FamPat2 PubMed: Desgrouas 2025 sib F yes France - 00y00m00d - - - ? see paper; ..., 13wg-antenatal ultrasound microcephaly, lower limb in hyperextension; birth 37wg, weight 1760 g, microcephaly (OFC 24.5 cm), incomplete Pierre Robin sequence (mandibular hypoplasia, glossoptosis, upper airway obstruction without cleft palate), clubfoot, camptodactylia, pulmonary hypoplasia; deceased minutes after birth, limbs malformation, severe microcephaly, dysmorphic features face (broad nasal root, flat face, deep crease philtrum, long thin upper lip, large ears), brain impairment cortical development, absence of layer organisation, deep columns of defective migrating cells 1 1 Johan den Dunnen
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