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Early prenatal presentation of the cartilage-hair hypoplasia / anauxetic dysplasia spectrum of disorders mimicking recurrent thanatophoric dysplasia.
Hall, Christine M; Liu, Becky; Haworth, Andrea; Reed, Laura; Pryce, Jeremy; Mansour, Sahar.
Afiliación
  • Hall CM; St George's, University of London, UK; Emeritus, Department of Radiology, Great Ormond Street Hospital, London, UK.
  • Liu B; Fetal Medicine Unit, St George's University Hospitals NHS Foundation Trust, London, UK.
  • Haworth A; Congenica Limited, Biodata Innovation Centre, Wellcome Genome Campus, Cambridge, UK.
  • Reed L; Congenica Limited, Biodata Innovation Centre, Wellcome Genome Campus, Cambridge, UK.
  • Pryce J; Department of Pathology, St George's University Hospitals NHS Foundation Trust, UK.
  • Mansour S; St George's, University of London, UK; SW Thames Regional Genetics Service, St George's University Hospitals NHS Foundation Trust, UK. Electronic address: smansour@sgul.ac.uk.
Eur J Med Genet ; 64(3): 104162, 2021 Mar.
Article en En | MEDLINE | ID: mdl-33567347
ABSTRACT
Three sibling fetuses identified with limb shortening and thoracic narrowing at twelve weeks' gestation on first trimester ultrasound examination are presented. The parents were non-consanguineous, Caucasian, healthy, of normal stature and had a healthy normal daughter. The radiographic abnormalities were highly suggestive of thanatophoric dysplasia, but molecular analysis failed to identify a pathogenic variant in FGFR3. The three fetuses were found to have identical compound heterozygous mutations in RMRP in trans, one inherited from the mother and one from the father. This represents the early prenatal presentation and fetal findings of metaphyseal dysplasia type McKusick (Cartilage-hair hypoplasia; CHH)/anauxetic dysplasia spectrum of disorders.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Displasia Tanatofórica / Pruebas Genéticas / Ultrasonografía Prenatal / Enanismo / Enfermedades de Inmunodeficiencia Primaria / Cabello / Enfermedad de Hirschsprung Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Displasia Tanatofórica / Pruebas Genéticas / Ultrasonografía Prenatal / Enanismo / Enfermedades de Inmunodeficiencia Primaria / Cabello / Enfermedad de Hirschsprung Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans / Pregnancy Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido