Anatomia funzionale del sistema nervoso dell'uomo by John Nolte

By John Nolte

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Dermal sinus 5. Encephalocele 6. ) 7. Hallermann-Streiff S. ) 8. Hypertelorism with Sprengel’s deformity 9. Parietal foramina; occipital foramina 10. Parietal thinning 11. Pyknodysostosis 12. Stanescu dysostosis 13. ) LETHAL ENTITIES WITH DEFECTIVE CRANIAL OSSIFICATION 1. Achondrogenesis, type I 2. Fibrochondrogenesis 3. Hypochondrogenesis 4. Hypophosphatasia (prenatal form; severe congenital form) 5. ) References 1. Campbell JB: Personal communication. 2. Dorst JP: Personal communication. Gamut A-38 SMALL ANTERIOR FONTANELLE 1.

Gamut A-26 ENLARGED, ERODED, OR DESTROYED SELLA TURCICA (INCLUDING INTRASELLAR OR PARASELLAR MASS ON CT OR MRI) COMMON 1. Aneurysm or ectatic internal carotid artery (cavernous or suprasellar segment); carotid-cavernous fistula 2. Craniopharyngioma 3. Cretinism; hypothyroidism 4. Empty sella syndrome; hypopituitarism 5. Increased intracranial pressure, chronic (eg, obstructive hydrocephalus; dilated third ventricle {aqueductal stenosis}; neoplasm; universal craniosynostosis) 6. Juxtasellar or suprasellar neoplasm, other (eg, meningioma; schwannoma of cranial nerves III to VI; optic chiasm glioma; epidermoid; dermoid; teratoma; hamartoma of tuber cinereum; hypothalamic glioma; germinoma; ectopic pinealoma) 7.

Petrositis or osteomyelitis, chronic 20 Gamut A-17 GENERALIZED INCREASED DENSITY, SCLEROSIS, OR THICKENING OF THE BASE OF THE SKULL (SEE A-16) COMMON 1. Fibrous dysplasia 2. Paget’s disease UNCOMMON 1. Anemiag, primary (eg, thalassemia; sickle cell disease; pyruvate kinase deficiency; hereditary spherocytosis) 2. Cleidocranial dysplasia 3. Craniodiaphyseal dysplasia 4. Craniometaphyseal dysplasia; frontometaphyseal dysplasia 5. Cretinism; hypothyroidism 6. Diaphyseal dysplasia (Camurati-Engelmann disease) 7.

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