- 1968.
Vohwinkel syndrome (also
known as "Keratoderma
hereditaria mutilans", "Keratoma
hereditaria mutilans", "Mutilating
keratoderma of Vohwinkel",: 213 ...
-
Dyschromatosis universalis hereditaria is a type of
pigmentation disorder of the skin. It is
characterized by dark and
light spots formed like lace in...
-
Dyschromatosis symmetrica hereditaria (also
known as "reticulate
acropigmentation of Dohi", and "symmetrical
dyschromatosis of the extremities") is a...
- A
captaincy (Spanish: capitanía [kapitaˈni.a], Portuguese:
capitania [kɐpitɐˈni.ɐ], Croatian: kapetanija) is a
historical administrative division of the...
- (1956). "Infantile
genetic agranulocytosis;
agranulocytosis infantilis hereditaria". Acta Paediatr. 45 (Suppl 105): 1–78. doi:10.1111/j.1651-2227.1956.tb06875...
-
hereditarias, y
constituian la
verdadera hidalguía del país; mas del dia, si bien en
algunas provincias todavía se
tramiten por
sucesion hereditaria,...
- the
legitimate heir of the
historic dynasty." "La
Corona de España es
hereditaria en los
sucesores de S. M. Don Juan
Carlos I de Borbón, legítimo heredero...
- 2006). "Dystonia,
mental deterioration, and
dyschromatosis symmetrica hereditaria in a
family with ADAR1 mutation".
Movement Disorders. 21 (9): 1510–1513...
-
Keratoendotheliitis fugax hereditaria is an
autosomal dominantly inherited disease of the cornea,
caused by a
point mutation in
cryopyrin (also known...
-
Hyperkalemic periodic paralysis (HYPP, HyperKPP) is an
inherited autosomal dominant disorder that
affects sodium channels in
muscle cells and the ability...
