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

Gkourogianni, Alexandra (author)
Karolinska Institutet
Andrade, Anenisia C. (author)
Division of Pediatric Endocrinology, Department of Women's and Children's Health, Karolinska Institute and University Hospital, Stockholm, Sweden; Center for Molecular Medicine, Karolinska Institute and University Hospital, Stockholm, Sweden
Jonsson, Björn-Anders (author)
Umeå universitet,Medicinsk och klinisk genetik
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Segerlund, Emma (author)
Department of Pediatrics, Sunderby Hospital, Sunderby, Sweden
Werner-Sperker, Antje (author)
Department of Pediatrics, Sunderby Hospital, Sunderby, Sweden
Horemuzova, Eva (author)
Karolinska Institutet
Dahlgren, Jovanna, 1964 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
Burstedt, Magnus (author)
Umeå universitet,Medicinsk och klinisk genetik
Nilsson, Ola, 1970- (author)
Karolinska Institutet,Örebro universitet,Institutionen för medicinska vetenskaper,Division of Pediatric Endocrinology, Department of Women's and Children's Health, Karolinska Institute and University Hospital, Stockholm, Sweden; Center for Molecular Medicine, Karolinska Institute and University Hospital, Stockholm, Sweden; University Hospital, Örebro, Sweden
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 (creator_code:org_t)
2020-03-06
2020
English.
In: Acta Paediatrica. - : Wiley-Blackwell Publishing Inc.. - 0803-5253 .- 1651-2227. ; 109:10, s. 2067-2074
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • AIM: To explore the phenotype and response to growth hormone in patients with heterozygous-mutations in the insulin-like growth factor I receptor gene (IGF1R).METHODS: Children with short-stature, microcephaly, born SGA combined with biochemical sign of IGF-I insensitivity were analyzed for IGF1R mutations or deletions using Sanger sequencing and Multiple ligation dependent probe amplification analysis.RESULTS: In two families, a novel heterozygous non-synonymous missense IGF1R variant was identified. In family 1, c.3364G>T, p.(Gly1122Cys) was found in the proband and co-segregated perfectly with the phenotype in three generations. In family 2, a de novo variant c.3530G>A, p.(Arg1177His) was detected. Both variants were rare, not present in the GnomAD database. Three individuals carrying IGF1R mutations have received rhGH treatment. The average gain in height SDS during treatment was 0.42 (range: 0.26 - 0.60) and 0.64 (range: 0.32 - 0.86) after 1 and 2 years of treatment, respectively.CONCLUSION: 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.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Medical Genetics (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Keyword

IGF1R
GH treatment
IGF-I
IGFBP-3
Idiopathic short stature
GH treatment
idiopathic short stature
IGF-I
IGF1R
IGFBP-3

Publication and Content Type

ref (subject category)
art (subject category)

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