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Spotted bones in an osteopoikilosis-related disease (Buschke Ollendorff Syndrome): Identifying this rare condition from the lab to the field.
Zdral, Sofía; Trujillo-Tiebas, María José.
Afiliación
  • Zdral S; Physical Anthropology Unit, Department of Biology, Universidad Autónoma de Madrid, Calle Darwin 2, 2804, Madrid, Spain. Electronic address: sofia.zdral@unican.es.
  • Trujillo-Tiebas MJ; Department of Genetics, Instituto de Investigación Sanitaria, Hospital Universitario Fundación Jiménez Diaz, Avenida de los Reyes Católicos 2, 28040, Madrid, Spain. Electronic address: MJTrujillo@fjd.es.
Int J Paleopathol ; 34: 20-28, 2021 09.
Article en En | MEDLINE | ID: mdl-34098227
OBJECTIVE: To improve the differential diagnosis of osteopoikilosis in past populations using a clinical case as an example of this rare condition. MATERIALS: A patient referred to our Genetic Service with suspected Buschke Ollendorff Syndrome after finding a connective nevus. METHODS: Radiological images from different body regions were accompanied by a genetic study using next-generation sequencing. RESULTS: Small circular-to-ellipsoid sclerotic lesions were found in the epiphysis and metaphysis of long bones, as well as in the pelvis. These lesions were bilaterally distributed and with well-defined margins, compatible with the characteristics of Buschke Ollendorff Syndrome, bone manifestation osteopoikilosis. A heterozygous mutation on LEMD3 (NM_001167614:c.1918 + 1G > C) was identified by next-generation sequencing. Based on this confirmed case, we have discussed the most probable causes of similar bone lesions found in the archaeological record. CONCLUSION: It has been demonstrated how a current case of a rare disease can provide useful tools to improve the differential diagnosis of this disease in ancient skeletons. SIGNIFICANCE: This work underlines the great need for multidisciplinary platforms that integrates clinical research into paleopathology in order to successfully address the study of rare diseases from the past. LIMITATIONS: Since OPK is only detected by X-rays, suspected cases of this bone lesion will only be identified when radiographs are taken for other purposes. SUGGESTIONS FOR FURTHER RESEARCH: Retrospective and large-scale studies of radiographs from other research in past populations.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteopoiquilosis / Enfermedades Cutáneas Genéticas Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Int J Paleopathol Año: 2021 Tipo del documento: Article Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteopoiquilosis / Enfermedades Cutáneas Genéticas Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Int J Paleopathol Año: 2021 Tipo del documento: Article Pais de publicación: Países Bajos