-
Dwarfism is a
condition wherein an
organism is
exceptionally small, and
mostly occurs in the
animal kingdom. In humans, it is
sometimes defined as an adult...
- bone
dysplasia with
cloverleaf skull Mosaic trisomy 5
Muenke syndrome Osteoglophonic dysplasia Pfeiffer syndrome Thanatophoric dysplasia,
types 1 and 2 Carpenter...
- ****ociated Jackson–Weiss syndrome, Antley-Bixler syndrome, Trigonocephaly,
osteoglophonic dysplasia,
squamous cell lung
cancer and
autosomal dominant Kallmann...
-
contractures Osteogenesis imperfecta retinopathy Osteogenic sarcoma Osteoglophonic dwarfism Osteolysis hereditary multicentric Osteolysis syndrome recessive...
-
CRTAP genes.[citation needed]
Pfeiffer syndrome Osteogenesis imperfecta Osteoglophonic dwarfism There is no
specific treatment for this
condition currently...
- (Concept Id: C4302879)". www.ncbi.nlm.nih.gov.
Retrieved 2023-07-06. "
Osteoglophonic dysplasia (Concept Id: C0432283)". www.ncbi.nlm.nih.gov.
Retrieved 2023-07-03...
- 372nd
amino acid of FGFR1 (Y372C) is
responsible for some
cases of
Osteoglophonic dysplasia. This
mutation results in craniosynostosis,
mandibular prognathism...
- VII; 610682;
CRTAP Osteogenesis imperfecta, type VIII; 610915; LEPRE1
Osteoglophonic dysplasia; 166250; FGFR1 Osteolysis,
familial expansile; 174810; TNFRSF11A...
-
Cleidocranial dyspalsia, Osteoporosis,
Rutherford syndrome, GAPO
syndrome and
Osteoglophonic dysplasia. Decker, Eva; Stellzig-Eisenhauer, Angelika; Fiebig, Britta...
