Case Report
Year 2017,
Volume: 5 Issue: 2, 27 - 31, 31.08.2017
Abstract
Abstract:
Pallister-Killian syndrome
(PKS) is an extremely rare medical condition characterized by tetrasomy of P
arm in 12th chromosome Individuals with this condition have also
isochromosomic mosaicism. Pigmentation disorders mental retardation, seizures
and hypotonia are common features of the syndrome. Anatomic malformation such
as extremity deformities, short neck, frontal bossing, cardiac and renal
pathologies are hallmark of clinical presentation in PKS. Here, we present a
two-month-old boy with typical case of PKS, and would like to increase
attention to Pallister-Killian Syndrome.
Keywords
References
- 1. Nelson pediateri, İnsan genetiği, Bölüm 75 sitogenetik, 76.6 mozaisizim 412
- 2. Pallister PD, Meisner LF, Elejalde BR, et al. The Pallister mosaic syndrome. Birth Defects 1977;XIH(3B): 103-10.
- 3. Fryns JP, Petit P, Vinken L, Geutjwns J, Marien J, Van den Berghe H. Mosaic tetrasomy 21 in severe mental handicap. Eur J Pediatr 1982;139: 87-9.
- 4. Hunter AGW, Clifford B, Speevak M, MacMurray SB. Mosaic tetrasomy 21 in liveborn male infant. Clin Genet 1982;21: 228-32.
- 5. Kwee ML, Barth PG, Arwert F, Madan K. Mosaic tetrasomy 21 in a male child. Clin Genet 1984;26: 150-5.
- 6. Harrod MJE, Howard-Peebles PN, Friedman JM. Tetrasomy 12p: differential degree of mosaicism in fibroblasts from normal and abnormally pigmented skin. Proc Greenwood Genet Center 1987;6: 107.
- 7. Killian W, Teschier-Nicola M. Case report 72: mental retardation, unusual facial appearance, abnormal hair. Synd Ident 1981;7: 6-7.
- 8. Wenger SL, Steele MW, Yu WD. Risk effect of maternal age in Pallister i(12p) syndrome. Clin Genet 1988;34: 181-4
- 9. Schinzel A, Tetrasomy 12p (Pallister-Killian syndrome). J Med Genet 1991; 28: 122-125
- 10. Reynolds JF, Daniel A, Kelly TE, et al. Isochromosome 12p mosaicism (Pallis-ter mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases. Am Med Ge-net 1987;27: 257-74.
- 11. Ward BE, Hayden MW, Robinson A. Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis. AmJ Med Ge-net 1988;31: 835-9.
- 12. Lin AE, Clemens M, Garver KL, Wenger S. Case of PallisterKillian syndrome with imperforate anus. Am Med Genet 1988;31: 705-7.13. Gilgenkrantz S, Droulle P, Schweitzer M, et al. Mosaic tetrasomy 12p. Clin Ge-net 1985;28: 495-502.
- 14. Naharara K, Wakita Y, Kikkawa K, et al. Pallister-Killian syndrome: cytogenetic and biochemical studies. Jpn Hum Genet 1988;33: 339-47.
- 15. Pauli RM, Zeier RA, Sekhon GS. Mosaic isochromosome 12p. Am Med Genet 1987;27: 291-4.
Year 2017,
Volume: 5 Issue: 2, 27 - 31, 31.08.2017
Abstract
References
- 1. Nelson pediateri, İnsan genetiği, Bölüm 75 sitogenetik, 76.6 mozaisizim 412
- 2. Pallister PD, Meisner LF, Elejalde BR, et al. The Pallister mosaic syndrome. Birth Defects 1977;XIH(3B): 103-10.
- 3. Fryns JP, Petit P, Vinken L, Geutjwns J, Marien J, Van den Berghe H. Mosaic tetrasomy 21 in severe mental handicap. Eur J Pediatr 1982;139: 87-9.
- 4. Hunter AGW, Clifford B, Speevak M, MacMurray SB. Mosaic tetrasomy 21 in liveborn male infant. Clin Genet 1982;21: 228-32.
- 5. Kwee ML, Barth PG, Arwert F, Madan K. Mosaic tetrasomy 21 in a male child. Clin Genet 1984;26: 150-5.
- 6. Harrod MJE, Howard-Peebles PN, Friedman JM. Tetrasomy 12p: differential degree of mosaicism in fibroblasts from normal and abnormally pigmented skin. Proc Greenwood Genet Center 1987;6: 107.
- 7. Killian W, Teschier-Nicola M. Case report 72: mental retardation, unusual facial appearance, abnormal hair. Synd Ident 1981;7: 6-7.
- 8. Wenger SL, Steele MW, Yu WD. Risk effect of maternal age in Pallister i(12p) syndrome. Clin Genet 1988;34: 181-4
- 9. Schinzel A, Tetrasomy 12p (Pallister-Killian syndrome). J Med Genet 1991; 28: 122-125
- 10. Reynolds JF, Daniel A, Kelly TE, et al. Isochromosome 12p mosaicism (Pallis-ter mosaic aneuploidy or Pallister-Killian syndrome): report of 11 cases. Am Med Ge-net 1987;27: 257-74.
- 11. Ward BE, Hayden MW, Robinson A. Isochromosome 12p mosaicism (Pallister-Killian syndrome): newborn diagnosis by direct bone marrow analysis. AmJ Med Ge-net 1988;31: 835-9.
- 12. Lin AE, Clemens M, Garver KL, Wenger S. Case of PallisterKillian syndrome with imperforate anus. Am Med Genet 1988;31: 705-7.13. Gilgenkrantz S, Droulle P, Schweitzer M, et al. Mosaic tetrasomy 12p. Clin Ge-net 1985;28: 495-502.
- 14. Naharara K, Wakita Y, Kikkawa K, et al. Pallister-Killian syndrome: cytogenetic and biochemical studies. Jpn Hum Genet 1988;33: 339-47.
- 15. Pauli RM, Zeier RA, Sekhon GS. Mosaic isochromosome 12p. Am Med Genet 1987;27: 291-4.
There are 14 citations in total.
Details
| Primary Language | English |
|---|---|
| Subjects | Health Care Administration |
| Journal Section | Case Reports |
| Authors | |
| Publication Date | August 31, 2017 |
| Acceptance Date | August 27, 2018 |
| Published in Issue | Year 2017 Volume: 5 Issue: 2 |