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Pre- and postnatal growth failure with microcephaly due to two novel heterozygous IGF1R mutations and response to growth hormone treatment.

Alexandra GkourogianniAnenisia C AndradeBjörn-Anders JonssonEmma SegerlundAntje Werner-SperkerEva HoremuzovaJovanna DahlgrenMagnus BurstedtOla Nilsson
Published in: Acta paediatrica (Oslo, Norway : 1992) (2020)
Our study presents two heterozygous IGF1R mutations causing pre- and postnatal growth failure and microcephaly and also indicates that individuals with heterozygous IGF1R mutations can respond to rhGH treatment. The findings highlight that sequencing of the IGF1R should be considered in children with microcephaly and short stature due to pre- and postnatal growth failure.
Keyphrases
  • growth hormone
  • zika virus
  • intellectual disability
  • preterm infants
  • early onset
  • pi k akt
  • single cell
  • autism spectrum disorder
  • cell proliferation