-
Poikiloderma is a skin
condition that
consists of
areas of hypopigmentation, hyperpigmentation,
telangiectasias and atrophy.
Poikiloderma of
Civatte is...
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Poikiloderma vasculare atrophicans (PVA), is a
cutaneous condition (skin disease)
characterized by hypo- or
hyperpigmentation (diminished or heightened...
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Kindler syndrome (also
known as "bullous
acrokeratotic poikiloderma of
Kindler and Weary") is a rare
congenital disease of the skin
caused by a mutation...
- has been
implicated in the syndrome. Sun-sensitive rash with
prominent poikiloderma and
telangiectasias Juvenile cataracts Saddle nose
Congenital bone defects...
-
Poikiloderma of
Civatte is a
cutaneous condition and
refers to
reticulated red to red-brown skin
patches with telangiectasias. It is
identifiable as a...
- Naegeli–Franceschetti–Jad****ohn
syndrome (NFJS), also
known as chromatop****
nevus of
Naegeli and
Naegeli syndrome, is a rare
autosomal dominant form of...
- Side
effects may be mild such as itchiness, folliculitis, sunburn,
poikiloderma, and a
theoretical risk of
nonmelanoma cancer or
melanoma has been suggested...
-
Incontinentia pigmenti (IP) is a rare X-linked
dominant genetic disorder that
affects the skin, hair, teeth,
nails and
central nervous system. It is named...
- hours)
Granuloma Livedo Purpura Erythema (redness) Horn (a cell type)
Poikiloderma Hyperkeratosis Parakeratosis Hypergranulosis Acanthosis Papillomatosis...
-
poikiloderma,
bullous acrokeratotic poikiloderma of
Kindler and Weary,
congenital poikiloderma with
blisters and keratoses,
congenital poikiloderma with...
