od strane Radmin | мар 31, 2023 | Bolesti
Vaskulitis predstavlja klinički heterogenu skupinu bolesti multifaktorijalne etiologije koju karakteriše upala bilo velikih krvnih sudova (vaskulitis velikih sudova, npr. Giant-ćelijski arteritis i Takayasu arteritis; videti ove pojmove), srednje velikih krvnih...
od strane Radmin | мар 31, 2023 | Bolesti
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth.
od strane Radmin | мар 31, 2023 | Bolesti
Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.
od strane Radmin | мар 31, 2023 | Bolesti
Citrullinemia is an autosomal recessively inherited disorder of urea cycle metabolism and ammonia detoxification (see this term) characterized by elevated concentrations of serum citrulline and ammonia. The disease presents with a large range of manifestations...
od strane Radmin | мар 31, 2023 | Bolesti
DPAGT1-CDG is a form of congenital disorders of N-linked glycosylation characterized by hypotonia, intractable seizures, developmental delay, microcephaly and severe fetal hypokinesia. Additional features that may be observed include apnea and respiratory deficiency,...
od strane Radmin | мар 31, 2023 | Bolesti
Geroderma osteodysplastica (GO) is characterized by lax and wrinkled skin (especially on the dorsum of the hands and feet and abdomen), progeroid features, hip dislocation, joint laxity, severe short stature/dwarfism, severe osteoporosis, vertebral abnormalities and...
od strane Radmin | мар 31, 2023 | Bolesti
NULL
od strane Radmin | мар 31, 2023 | Bolesti
NULL
od strane Radmin | мар 31, 2023 | Bolesti
Actinic lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by the development of photo-distributed lichenoid lesions.
od strane Radmin | мар 31, 2023 | Bolesti
ALG11-CDG is a form of congenital disorders of N-linked glycosylation characterized by facial dysmorphism (microcephaly, high forehead, low posterior hairline, strabismus), hypotonia, failure to thrive, intractable seizures, developmental delay, persistent vomiting...
