DeSanctis–Cacchione syndrome is a genetic disorder characterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring in association with...

organizational theorist De Sanctis (disambiguation) DeSantis DeSanctis–Cacchione syndrome This page lists people with the surname DeSanctis. If an internal link...

3268 De Sanctis (1981 DD), Main-belt Asteroid discovered in 1981 De Locis Sanctis, book by the Irish monk Adomnán DeSanctis–Cacchione syndrome, an extremely...

treatments and prevention for cancer. DeSanctis–Cacchione syndrome Genetic disorder Biogerontology Cockayne syndrome List of skin conditions List of cutaneous...

Denys–Drash syndrome DeSanctis–Cacchione syndrome Descending perineum syndrome Diabetic stiff hand syndrome Dialysis disequilibrium syndrome Diencephalic...

pigmentosa-Cockayne syndrome (XP-CS). Variants of these diseases, such as DeSanctis–Cacchione syndrome and Cerebro-oculo-facio-skeletal (COFS) syndrome, can also...

syndrome De Barsy syndrome De Hauwere–Leroy–Adriaenssens syndrome DeSanctis–Cacchione syndrome Deaf blind hypopigmentation Deafness Deafness c – Deafness...

Bloom syndrome (often abbreviated as BS in literature) is a rare autosomal recessive genetic disorder characterized by short stature, predisposition to...

Werner syndrome (WS) or Werner's syndrome, also known as "adult progeria", is a rare, autosomal recessive disorder which is characterized by the appearance...

Cockayne syndrome (CS), also called Neill-Dingwall syndrome, is a rare and fatal autosomal recessive neurodegenerative disorder characterized by growth...

a specific type of progeroid syndrome, also known as Hutchinson–Gilford syndrome or Hutchinson–Gilford progeroid syndrome (HGPS). A single gene mutation...

Rothmund–Thomson syndrome (RTS) is a rare autosomal recessive skin condition. There have been several reported cases associated with osteosarcoma. A hereditary...

initials of the words involved. BIDS syndrome, also called Amish brittle hair brain syndrome and hair-brain syndrome, is an autosomal recessive inherited...

Marfanoid–progeroid–lipodystrophy syndrome (MPL), also known as Marfan lipodystrophy syndrome (MFLS) or progeroid fibrillinopathy, is an extremely rare...

syndrome Crouzon syndrome Cutis verticis gyrata Darier's disease (Darier–White disease, dyskeratosis follicularis, keratosis follicularis) DeSanctis–Cacchione...

Dyskeratosis congenita (DKC), also known as Zinsser-Engman-Cole syndrome, is a rare progressive congenital disorder with a highly variable phenotype. The...

De Barsy syndrome is a rare autosomal recessive genetic disorder. Symptoms include cutis laxa (loose hanging skin) as well as other eye, musculoskeletal...

Wiedemann–Rautenstrauch (WR) syndrome (German pronunciation: [ˈviːdəman ˈʁaʊtn̩ʃtʁaʊx]), also known as neonatal progeroid syndrome, is a rare autosomal recessive...

is a rare, lethal autosomal recessive skin condition characterized by syndromic facies, tight skin, sparse or absent eyelashes, and secondary joint changes...

Darsun syndrome; 612541; G6PC3 D-bifunctional protein deficiency; 261515; HSD17B4 De la Chapelle dysplasia; 256050; SLC26A2 De Sanctis–Cacchione syndrome; 278800;...