-
character of the Night's Dawn
trilogy and also :
Folliculitis rubra, a
genodermatose Granulosis rubra nasi, a rare
familial disease of
children occurring...
-
acral erythema Necrolytic migratory erythema (glucagonoma syndrome)
Genodermatoses are
inherited genetic skin
conditions often grouped into
three categories:...
-
Epidermolysis bullosa dystrophica or
dystrophic EB (DEB) is an
inherited disease affecting the skin and
other organs. "Butterfly child" is the colloquial...
-
Epidermolysis bullosa (EB) is a
group of rare
medical conditions that
result in easy
blistering of the skin and
mucous membranes.
Blisters occur with minor...
- Von Hippel–Lindau
disease (VHL), also
known as Von Hippel–Lindau syndrome, is a rare
genetic disorder with
multisystem involvement. It is characterized...
-
Keratosis pilaris (KP; also
follicular keratosis,
lichen pilaris, or
colloquially chicken skin.) is a common, autosomal-dominant,
genetic condition of...
- Dirk; Treat,
James R.; Rosenbach,
Misha A.; Neuhaus,
Isaac (2020). "27.
Genodermatoses and
congenital anomalies". Andrews'
Diseases of the Skin:
Clinical Dermatology...
-
Heterochromia is a
variation in
coloration most
often used to
describe color differences of the iris, but can also be
applied to
color variation of hair...
- (2019, June).
Types of
Genodermatoses.
Retrieved September 08, 2020, from https://www.news-medical.net/health/Types-of-
Genodermatoses.aspx Bayart, Cheryl...
- S2CID 8824095. Cohen, P. R.; Kurzrock, R. (1995-01-01). "Miscellaneous
genodermatoses: Beckwith-Wiedemann syndrome, Birt-Hogg-Dube syndrome,
familial atypical...
