Crouzon syndrome

Growth

Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus. The patient"s bone age was only 4. 5-5 years according to the Greulich and Pyle atlas.

Growth

Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus. MRI revealed obstructive hydrocephalus of both lateral ventricles, shallow orbits, and cerebellar tonsil herniation (Chiari I malformation). Pituitary height was 5.6 mm in midsagittal T1-weighted spin-echo MRI.

An inherited

FGFR2 mutation increased osteogenesis gene expression and result in Crouzon syndrome. Crouzon syndrome patients and morphology measurement of orbit. a Five-generation Crouzon syndrome pedigree. Affected individuals are indicated by filled symbols, the proband is marked with an upward arrow. b Facial photographs of the Crouzon syndrome patients. c Morphology measurement of orbit. (Ca) Three-dimensional reconstruction of skull of the proband IV-2 (Cb) Morphology measurement of orbit(a. midinterorbital distance, b.lateral orbital wall angle) (Cc) Morphology measurement of orbit(a. roof length, b. medial wall length, c. floor length, d. lateral wall length, e. orbital width, f. orbital height)

Inherited

FGFR2 mutation in a Chinese patient with Crouzon syndrome and luxation of bulbus oculi provoked by trauma: a case report. Patients with Crouzon syndrome and clinical examination of the proband. a Three-generational Crouzon syndrome pedigree. Affected individuals are indicated by filled symbols and the proband is marked with an arrow. b, c Computed tomography and magnetic resonance imaging did not reveal retrobulbar hematoma and revealed shallow orbits and obvious ocular proptosis in the proband. d Facial photographs of patients with Crouzon syndrome

Crouzon

syndrome • Crouzon syndrome - Ganzer Fall bei Radiopaedia