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Dyskeratosis congenita (DKC), also
known as Zinsser-Engman-Cole syndrome, is a rare
progressive congenital disorder with a
highly variable phenotype. The...
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Dyskeratosis is
abnormal keratinization occurring prematurely within individual cells or
groups of
cells below the
stratum granulosum.
Dyskeratosis congenita...
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characterized by
excessively short telomeres and is
considered a
severe form of
dyskeratosis congenita.
Being an X-linked disorder, Hoyeraal–Hreid****on
syndrome primarily...
- patches, also
known as
keratotic pa****s,
keratosis follicularis, or
dyskeratosis follicularis, most
often appear on the arms, chest, back and legs. DD...
- been
negatively affected by
upper respiratory tract disease,
cutaneous dyskeratosis,
herpes virus, s**** necrosis,
urolithiasis (bladder stones), and parasites...
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Familial disseminated comedones without dyskeratosis (FDCWD) is a rare
autosomal dominant skin
disorder characterized by the
presence of
numerous comedones...
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dermatosis characterized histologically by acantholysis: 529 with or
without dyskeratosis. Once confirmed, most
cases of Grover's
disease last six to
twelve months...
- has been
suggested as a
cause or
contributing factor of this disease.
Dyskeratosis congenita (DC) is a
disease of the bone
marrow that can be
caused by...
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Hereditary benign intraepithelial dyskeratosis is a rare
autosomal dominant disease of the
conjunctiva and the oral
mucosa caused by a
duplication of chromosome...
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underpins most Diamond–Blackfan
anemia (DBA), the X-linked
subtype of
dyskeratosis congenita (DKCX),
Treacher Collins syndrome (TCS), Shwachman–Diamond...
