Manifestasi sistemis dan oral sindrom turner
Nomor Panggil : 612.3 REN m
Penerbit : FKG - Usakti
Kota Terbit : Jakarta
Tahun Terbit : 2006
Pembimbing 1 : Janti Sudiono
Subyek : Oral biology;Turner's syndrome
Kata Kunci : turner syndrome, X chromosome, short stature, turner tooth.
Status Posting : Published
Status : Lengkap
No. | Nama File | Hal. | Link |
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1. | 2006_TA_KG_04003171_Halaman-judul.pdf | 9 | |
2. | 2006_TA_KG_04003171_Lembar-pengesahan.pdf | 1 | |
3. | 2006_TA_KG_04003171_Bab-1-Pendahuluan.pdf | 2 | |
4. | 2006_TA_KG_04003171_Bab-2-Tinjauan-pustaka.pdf | 66 |
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5. | 2006_TA_KG_04003171_Bab-3-Pembahasan.pdf | 15 |
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6. | 2006_TA_KG_04003171_Bab-4-Kesimpulan-dan-saran.pdf | 6 |
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7. | 2006_TA_KG_04003171_Daftar-pustaka.pdf | 1 |
S Sindrom Turner adalah suatu kelainan kromosom yang biasa terjadi pada wanita yang disebabkan oleh kehilangan sebagian atau seluruh dari kromosom X. Sindrom Turner dapat dibagi menjadi 2 macam yaitu sindrom Turner klasik dan sindrom Turner mosaik. Adapun etiologinya adalah kerusakan karakteristik dari kromosom X. Manifestasi sistemis dan oral yang khas antara lain : tubuh pendek (.1/Jort stature), leher berselaput, dada berbentuk perisai, pectus excavatum, sk1J{iosis, cubitm valgus, koarktasio aorta, bicuspid aortic valve, horseshoe kidney, ptosis, strabismus, kelainan pembentukan ovarium, kclainan psikologis, kelainan pendengaran, diabetes, penyakit tiroid, lengkung palatum yang dalam, hipoplasia mandibula, erupsi dini gigi permanen, maloklusi, gigi Turner, mikrognatia, perubahan bentuk dan ukuran gigi. Sindrom Turner dapat didiagnosis dengan beberapa pemeriksaan yaitu chorionic villous sampling atau amniocentesis, penyaringan serum ibu yang tidak nonnal, dengan ultrasound dan tes karyotype. Diagnosis manifestasi oralnya melalui pemeriksaan klinis dan radiografi. Prognosis dan perawatan sangat tergantung pada manifestasi manifestasi yang terjadi.
T Turner syndrome is a chromosomal disorder which usually affecting females wherein one of the two X-chromosomes is defective or completely absent. Turner s:-ndrome can be divided into two type: Turner syndrome clasic and Turner syndrome mosaic. The etiology of Turner syndrome is assosiated ,vith characteristic defect in the X-chromosome. The spesific sistemic and oral manifestations are short stature, webbed neck, shield-like chest, pectus e:-,;cavatum, scoliosis, cubitus valgus, coarctation of the aorta, bicuspid aortic valve, horseshoe kidney, ptosis, strabismus, ovarian failure, psychological abnonnalities, hearing abnormalities, diabetes, thyroid disease, high-arched palate, hypoplastic mandible, early eruption of permanent teeth, malocclusion, Turner tooth, micrognathia, change in shape and size of tooth. Tuner syndrome can be diagnosed through several examinations such as chorionic villous sampling or amniocentesis, abnormal maternal serum screening, ultrasound and karyotype test. The oral manifestation can be diagnosed by clinical and radiograph e,aminations. Prognosis and treatment are depended on the manifestations that happening.