Öz
Tongue is the most mobile organ of the body with multiple functions such as speech, mastication, taste and swallowing. Numerous congenital and developmental disorders of the tongue have been reported in literature. Hypoglossia also known as microglossia is one of the rare anomalies. Usually hypoglossia is associated with many other systemic abnormalities but rarely found as an isolated entity. Lack of tongue development leads to decreased mandibular growth. The aim of this article is to report a rare case of isolated hypoglossia and resultant micrognathia. Presence of palatal and faucial pillar abnormalities with hypoglossia which is extremely rare is also highlighted in our report.
Anahtar Kelimeler
Kaynakça
- Shafer WG, Hine MK and Levy BM. A textbook of oral pathology. Philadelphia: WB Saunders Company, 2003. pp. 24.
- Rachmiel A, Jackson IT, Sabapathy SR and Forte RA. Severe congenital hypoplasia of tongue and abnormal shape of soft palate and tonsillar pillar. Eur J Plast Surg 1993;16(3):149-53.
- Kumar P and Chaubey KK. Aglossia: A case report. J Indian Soc Pedod Prev Dent 2007;25(1): 46-48.
- Williams PL and Warwick R. Gray’s Anatomy. 30th edition. Churchill Livingstone, 1980. pp.13028.
- Grippaudo FR and Kennedy DC. Oromanibular-limb hypogenesis Syndrome; A case of aglossia with intraoral band. Br J Plast Surg; 1998; 51(6): 480-483.
- Jang GY, Lee KC, Joung JT, Son CS and Tockgo YC. Congenital Aglossia with situs inversus totalis- A case report. J Kor Med Sci, 1997;12(1): 55-57.
- Hall BD. Aglossia – adactylia. Birth defects, 1971;7: 233-236.
- Rasool A, Zaroo MI, Wani AH, Darzi MA, Bashir SA, Bijli AH and Rashid S. Isolated aglossia in a six year old child presenting with impaired speech: a case report. Cases journal, 2009;2: 1-3.
- Khalil KC, Dayal PK, Gopa Kumar R and Prasanth S. Aglossia: A case report. Quintiessence int 1995;26(5):359-360.
Öz
Dil; konuşma, çiğneme , tatma ve yutma gibi birçok fonksiyona sahip, vücudumuzun en hareketli organıdır. Literatürde dilin sayısız konjenital ve kalıtımsal bozuklukları bildirilmiştir. Mikroglossi olarak da bilinen hipoglossi nadir anomalilerden biridir. Çoğunlukla diğer sistemik anormalliklerle ilişkilidir ancak nadiren izole bir antite olarak bulunur. Dilin gelişmesindeki yokluk düşük mandibüler gelişmeye yol açar. Bu yazının amacı nadir bir izole hipoglossi ve sebep olduğu mikrognatiyi sunmaktır. Hastamızda çok çok nadir görülen hipoglossiye eşlik eden palatal ve faucial pillar anormallikler de vurgulanmıştır.
Anahtar Kelimeler
Kaynakça
- Shafer WG, Hine MK and Levy BM. A textbook of oral pathology. Philadelphia: WB Saunders Company, 2003. pp. 24.
- Rachmiel A, Jackson IT, Sabapathy SR and Forte RA. Severe congenital hypoplasia of tongue and abnormal shape of soft palate and tonsillar pillar. Eur J Plast Surg 1993;16(3):149-53.
- Kumar P and Chaubey KK. Aglossia: A case report. J Indian Soc Pedod Prev Dent 2007;25(1): 46-48.
- Williams PL and Warwick R. Gray’s Anatomy. 30th edition. Churchill Livingstone, 1980. pp.13028.
- Grippaudo FR and Kennedy DC. Oromanibular-limb hypogenesis Syndrome; A case of aglossia with intraoral band. Br J Plast Surg; 1998; 51(6): 480-483.
- Jang GY, Lee KC, Joung JT, Son CS and Tockgo YC. Congenital Aglossia with situs inversus totalis- A case report. J Kor Med Sci, 1997;12(1): 55-57.
- Hall BD. Aglossia – adactylia. Birth defects, 1971;7: 233-236.
- Rasool A, Zaroo MI, Wani AH, Darzi MA, Bashir SA, Bijli AH and Rashid S. Isolated aglossia in a six year old child presenting with impaired speech: a case report. Cases journal, 2009;2: 1-3.
- Khalil KC, Dayal PK, Gopa Kumar R and Prasanth S. Aglossia: A case report. Quintiessence int 1995;26(5):359-360.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Bölüm | Olgu Sunumu |
| Yazarlar | |
| Yayımlanma Tarihi | 1 Mart 2011 |
| Yayımlandığı Sayı | Yıl 2011 Cilt: 1 Sayı: 1 |