Hereditary multiple exostosis
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Pachajoa Londoño, Harry Mauricio
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Abstract
Multiple Hereditary Exostoses (HME) is an autossomal dominant disorder that exhibits
multiple benign osteocartilaginous bone tumours that arise near the ends of long
bones during childhood. The most common complaint is pain and the exostoses may
degenerate into chondrosarcomas.
We report a female patient who underwent a rehabilitation program to ease her
complaints caused by a large exostosis in the left femur and displayed an exostose
of the nasal septa, feature never described before in HME. Molecular study
confirmed a novel mutation on the EXT 1 gene. The mutation of a cytosine for a
guanine nucleotide in the position 830 on the exon 1 of the EXT 1 gene (c.830C
> G) caused the replacement of the serine aminoacid for a stop codon in the
position 277 of the protein.
Description
La exostosis múltiple hereditaria o osteocondromatosis
hereditaria es una enfermedad genética autosómica dominante causada por mutaciones en genes que codifican
la exostosina, EXT1 (8q24.1), EXT2 (11p11-p13) y EXT3
(19p). Se caracteriza por presentar múltiples proyecciones de hueso cubiertas por cartílago, principalmente en
las metáfisis de los huesos largos como el brazo y el
antebrazo, aunque también pueden involucrar a huesos
de la cintura escapular, pélvica y costillas, y en menor
grado a vértebras, esternón, columna y huesos de carpo
y tarso.
Palabras clave
RehabilitaciónCondrosarcomaExostosis Múltiple Hereditaria (EMH)Ciencias socio biomédicas
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Medical sciences
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Except where otherwised noted, this item's license is described as Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
