Phenotypes for disease #00710 (AGS2 (Aicardi-Goutieres syndrome, type 2 (AGS2)), OMIM:610181)

4 entries on 1 page. Showing entries 1 - 4.
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Individual ID     
0000044553 Microcephaly HP:0000252 - - Familial, autosomal recessive - - - - - Birgit Sikkema-Raddatz 00057265
0000267395 HPOTerms: (+) Motor delay,(+) Limb hypertonia,(+) Muscular hypotonia of the trunk,(+) Abnormal CNS myelination,(+) Abnormal myelination // 18 months old, motor developmental delay, unable to sit freely, muscular trunk hypotonia, increased muscle tone of the extremities, increased muscular reflexes, cMRI: myelinisation disorder in the region of the medullary canal, in the internal capsule and in the U-fibres on both sides, temporopolar, social development so far unremarkable - 18mo Unknown - - - - - Andreas Laner 00372066
0000274620 Neurological regression (Neurological) - Aicardi-Goutieres syndrome 2 Familial - - - - - LOVD 00380767
0000308363 brain magnetic resonance imaging: multiple intra cerebral calcifications on ct-scan; additional clinical featuresfeeding problems, short stature, seizures, spasticity, severe developmental delay - Aicardi-Goutieres syndrome 2 [MIM 610181] Familial, autosomal recessive 5y - - - - LOVD 00416853
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