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Ullrich-Turner phenotype with unusual manifestation in a patient with mosaicism 45,X/47,XX,+18.
Franceschini, P; Guala, A; Camerano, P; Franceschini, D; Vardeu, M P; Signorile, F.
Afiliación
  • Franceschini P; Istituto di Discipline Pediatriche, Servizio di Genetica Clinica, Università di Torino, Italy.
Am J Med Genet ; 62(1): 26-8, 1996 Mar 01.
Article en En | MEDLINE | ID: mdl-8779320
We report on a girl with Ullrich-Turner phenotype and 45,X/47,XX,+18 chromosomal mosaicism. Only two other patients with similar mosaicism have been reported, both girls with XY sex chromosome constitution. The face of the patient was highly asymmetric, the right side being almost normal, the left showing a typical Ullrich-Turner syndrome appearance. This clinical impression was strengthened by photographic doubling of both hemifaces. The patient had normal intelligence and did not show any stigmata of trisomy 18.
Asunto(s)
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosoma X / Anomalías Múltiples / Cromosomas Humanos Par 18 / Mosaicismo Límite: Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet Año: 1996 Tipo del documento: Article País de afiliación: Italia
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosoma X / Anomalías Múltiples / Cromosomas Humanos Par 18 / Mosaicismo Límite: Adult / Child / Female / Humans / Male Idioma: En Revista: Am J Med Genet Año: 1996 Tipo del documento: Article País de afiliación: Italia