Discordant fetal phenotype of hypophosphatasia in two siblings

Satoru Ikenoue, Kei Miyakoshi, Tomohiro Ishii, Yu Sato, Toshimitsu Otani, Yohei Akiba, Yoshifumi Kasuga, Daigo Ochiai, Tadashi Matsumoto, Yosuke Ichihashi, Yohei Matsuzaki, Kanako Tachikawa, Toshimi Michigami, Gen Nishimura, Kazushige Ikeda, Tomonobu Hasegawa, Mamoru Tanaka

Research output: Contribution to journalArticle

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Abstract

Hypophosphatasia (HPP) is an autosomal recessive metabolic disorder with impaired bone mineralization due to mutations in the ALPL gene. The genotype-phenotype correlation of this disorder has been widely described. Here, we present two affected siblings, whose fetal phenotypes were discordant. A 31-year-old Japanese woman, G0P0, was referred to our institution because of fetal micromelia. After obstetric counseling, the pregnancy was terminated at 21 weeks’ gestation. Post-mortem radiographs demonstrated severely defective mineralization of the skeleton. The calvarial, spinal, and tubular bones were mostly missing. Only the occipital bones, mandible, clavicles, ribs, one thoracic vertebra, ilia, and tibia were relatively well ossified. The radiological findings suggested lethal HPP. Genetic testing for genomic DNA extracted from the umbilical cord identified compound heterozygous mutations in the ALPL gene (c.532T>C, p.Y178H; c.1559delT, p.Leu520Argfs*86). c.532T>C was a novel variant showing no residual activity of the protein by the functional analysis. The parents were heterozygous carriers. In the next pregnancy, biometric values on fetal ultrasonography at 20 and 26 weeks’ gestation were normal. At 34 weeks, however, a small chest and shortening of distal long bones came to attention. The neonate delivered at 41 weeks showed serum ALP of <5U/L. Radiological examination showed only mild thoracic hypoplasia and metaphyseal mineralization defects of the long bones. ALP replacement therapy was introduced shortly after birth, and the neonate was discharged at day 22 without respiratory distress. Awareness of discordant fetal phenotypes in siblings with HPP precludes a diagnostic error, and enables early medical intervention to mildly affected neonates.

Original languageEnglish
Pages (from-to)171-174
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Volume176
Issue number1
DOIs
Publication statusPublished - 2018 Jan 1

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Hypophosphatasia
Siblings
Phenotype
Pregnancy
Newborn Infant
Bone and Bones
Early Medical Intervention
Thorax
Occipital Bone
Prenatal Ultrasonography
Ilium
Thoracic Vertebrae
Physiologic Calcification
Clavicle
Mutation
Umbilical Cord
Genetic Testing
Genetic Association Studies
Ribs
Diagnostic Errors

Keywords

  • discordant phenotype
  • hypophosphatasia
  • prenatal diagnosis
  • siblings
  • ultrasound

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Discordant fetal phenotype of hypophosphatasia in two siblings. / Ikenoue, Satoru; Miyakoshi, Kei; Ishii, Tomohiro; Sato, Yu; Otani, Toshimitsu; Akiba, Yohei; Kasuga, Yoshifumi; Ochiai, Daigo; Matsumoto, Tadashi; Ichihashi, Yosuke; Matsuzaki, Yohei; Tachikawa, Kanako; Michigami, Toshimi; Nishimura, Gen; Ikeda, Kazushige; Hasegawa, Tomonobu; Tanaka, Mamoru.

In: American Journal of Medical Genetics, Part A, Vol. 176, No. 1, 01.01.2018, p. 171-174.

Research output: Contribution to journalArticle

Ikenoue, S, Miyakoshi, K, Ishii, T, Sato, Y, Otani, T, Akiba, Y, Kasuga, Y, Ochiai, D, Matsumoto, T, Ichihashi, Y, Matsuzaki, Y, Tachikawa, K, Michigami, T, Nishimura, G, Ikeda, K, Hasegawa, T & Tanaka, M 2018, 'Discordant fetal phenotype of hypophosphatasia in two siblings', American Journal of Medical Genetics, Part A, vol. 176, no. 1, pp. 171-174. https://doi.org/10.1002/ajmg.a.38531
Ikenoue, Satoru ; Miyakoshi, Kei ; Ishii, Tomohiro ; Sato, Yu ; Otani, Toshimitsu ; Akiba, Yohei ; Kasuga, Yoshifumi ; Ochiai, Daigo ; Matsumoto, Tadashi ; Ichihashi, Yosuke ; Matsuzaki, Yohei ; Tachikawa, Kanako ; Michigami, Toshimi ; Nishimura, Gen ; Ikeda, Kazushige ; Hasegawa, Tomonobu ; Tanaka, Mamoru. / Discordant fetal phenotype of hypophosphatasia in two siblings. In: American Journal of Medical Genetics, Part A. 2018 ; Vol. 176, No. 1. pp. 171-174.
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