od strane Radmin | мар 31, 2023 | Bolesti
MAN1B1-CDG is a form of congenital disorders of N-linked glycosylation characterized by intellectual disability, delayed motor development, hypotonia and truncal obesity. Additional features include slight facial dysmorphism (hypertelorism, downslanting palpebral...
od strane Radmin | мар 31, 2023 | Bolesti
NULL
od strane Radmin | мар 31, 2023 | Bolesti
NULL
od strane Radmin | мар 31, 2023 | Bolesti
Carnosinemia is a very rare inherited disorder that presents with serum carnosinase deficiency.
od strane Radmin | мар 31, 2023 | Bolesti
DPM3-CDG is an extremely rare form of CDG syndrome (see this term) characterized clinically in the single reported case by muscle weakness, waddling gait and dilated cardiomyopathy (see this term).
