Gorlin–Goltz Syndrome with Multidisciplinary Approach of Treatment
Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma s...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Jayachandran Sadaksharam [verfasserIn] Amutha Velappan Annapoorni [verfasserIn] |
|---|
| Format: |
E-Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2019 |
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| Schlagwörter: |
multiple odontogenic keratocyst syndrome |
|---|
| Übergeordnetes Werk: |
In: Annals of the National Academy of Medical Sciences (India) - Thieme Medical and Scientific Publishers Pvt. Ltd., 2015, 55(2019), 04, Seite 213-218 |
|---|---|
| Übergeordnetes Werk: |
volume:55 ; year:2019 ; number:04 ; pages:213-218 |
| Links: |
Link aufrufen |
|---|
| DOI / URN: |
10.1055/s-0039-3402665 |
|---|
| Katalog-ID: |
DOAJ018759939 |
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Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. |
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Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. |
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Gorlin–Goltz syndrome, is an uncommon genetic condition characterized by the presence of multiple odontogenic keratocysts of jaws along with several other abnormal, cutaneous, ophthalmic, and osseous displays. This syndrome is also acknowledged by various names, such as nevoid basal cell carcinoma syndrome, jaw cyst, and bifid rib syndrome. This article illustrates about the clinical, radiological, and histological diagnostic findings and the multidisciplinary approach of treatment given to one such rare case of Gorlin–Goltz syndrome. |
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