Author(s): TylkiSzymaska A, Maciejko D, Kidawa M, JaboskaBudaj U, Czartoryska B
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Abstract This communication reports the clinical and biochemical results in six patients: four with mucopolysaccharidosis, one with GM1 gangliosidosis (Morquio B) and one with I-cell disease, who were treated by amniotic tissue transplantation. The sole evident clinical result was the diminishing of corneal clouding in three cases. A slight increase of beta-galactosidase activity in one patient's plasma was observed. The time of improvement was about 2 months after the transplantation and was transitory.
This article was published in J Inherit Metab Dis
and referenced in Journal of Stem Cell Research & Therapy