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Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1: A single-center case series of 15 patients and seven novel TRPS1 variants.
Herlin, Laura Krogh; Herlin, Morten Krogh; Blechingberg, Jenny; Rønholt, Kirsten; Graversen, Lise; Schmidt, Sigrun A J; Jørgensen, Mette Warming; Hellfritzsch, Michel Bach; Hald, Jannie Dahl; Beck-Nielsen, Signe Sparre; Gjørup, Hans; Andersen, Brian Nauheimer; Gregersen, Pernille Axél; Sommerlund, Mette.
Afiliación
  • Herlin LK; Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark. Electronic address: laujoerg@rm.dk.
  • Herlin MK; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Blechingberg J; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Rønholt K; Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark.
  • Graversen L; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Schmidt SAJ; Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Epidemiology, Aarhus University Hospital, Aarhus, Denmark.
  • Jørgensen MW; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
  • Hellfritzsch MB; Department of Radiology, Aarhus University Hospital, Aarhus, Denmark.
  • Hald JD; Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Beck-Nielsen SS; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Gjørup H; Centre for Oral Health in Rare Diseases, Department of Dental and Maxillofacial Surgery, Aarhus University Hospital, Aarhus, Denmark.
  • Andersen BN; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Gregersen PA; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark.
  • Sommerlund M; Department of Dermatology, Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Eur J Med Genet ; 69: 104937, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38574886
ABSTRACT
Tricho-rhino-phalangeal syndrome (TRPS) is a rare malformation syndrome characterized by distinctive facial, ectodermal, and skeletal features. TRPS is divided into TRPS type I/III caused by pathogenic variants in TRPS1 and TRPS type II caused by contiguous gene deletions also spanning EXT1 and RAD21. Due to its rarity, knowledge of the clinical course of TRPS remains limited. Therefore, we collected and characterized a case series of 15 TRPS type I patients (median age at diagnosis 15 [interquartile range 10-18] years, 11 females [73%]) seen at Aarhus University Hospital, Denmark, with a median follow-up period of 10 years. We estimated a minimum point prevalence of 0.5 in 100,000 (95% CI 0.3-0.8 per 100,000) persons. Common craniofacial features included fine and sparse hair with a high anterior hairline, eyebrows with lateral thinning and a thicker medial part, prominent ears, a bulbous nose tip with small nasal alae, a low-hanging, and often wide columella, and a long philtrum with a thin upper vermillion. Specific skeletal features included short stature and deviating and short fingers with cone-shaped epiphyses and shortened metacarpals on radiographs. The most significant morbidity of the cohort was joint complaints, which were reported by all patients, often already before the TRPS diagnosis was established. We identified ten different TRPS1 variants including both frameshift/nonsense, missense, and splice-site variants, including seven variants not previously reported in the literature. In accordance with previous literature, no genotype-phenotype correlation was identified. The clinical trajectories were heterogeneous involving pediatrics, dermatology, orthopedic surgery, clinical genetics, and/or odontology, emphasizing that close multidisciplinary collaboration is essential for early diagnosis of TRPS and to ensure proper and timely patient care and counseling.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Represoras / Factores de Transcripción / Síndrome de Langer-Giedion / Proteínas de Unión al ADN Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas Represoras / Factores de Transcripción / Síndrome de Langer-Giedion / Proteínas de Unión al ADN Límite: Adolescent / Child / Female / Humans / Male Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2024 Tipo del documento: Article