Page 62 - GPD-1-1

Gene & Protein in Disease Bangladesh genetic disease database

https://doi.org/10.3329/bmj.v43i1.21376 children and health burden of thalassemia in our population.
Dhaka Shishu Hosp J, 21(1): 1–7.
83. Tabib S, Halim M, Islam M, 1996, Osteopetrosis - A case
report. Bangladesh J Med Sci, 3(1): 27–31. 96. Pervin S, Sultana H, Ahmed T, et al., 2021, Knowledge and
awareness regarding premarital screening of β-thalassemia
https://doi.org/10.3329/bjms.v3i1.8224
among undergraduate students in Bangladesh. J Curr Med
84. Barua M, Rashid M, Rouf MA, et al., Pachydermoperiostosis: Res Opin, 4(1): 730–737.
A rare genetic disorder. BIRDEM Med J, 8(2): 181–183.
https://doi.org/10.15520/jcmro.v4i01.379
https://doi.org/10.3329/birdem.v8i2.36652
97. Rahman MM, Khan L, 2017, Co-inheritance of α- and
85. Bhuiyan MR, Ali NF, Sultana A, et al., 2012, A primary β-thalassemia in a Bangladeshi family. Bangabandhu Sheikh
hypertrophic osteoarthropathy or pachydermoperiostosis. Mujib Med Univ J, 10(2): 123.
Mymensingh Med J, 21(3): 557–61.
https://doi.org/10.3329/bsmmuj.v10i2.32708
86. Ahmmed MF, Shazzad MN, Ferdous S, et al.,
2017, Polyarthritis is a rare manifestation of 98. Siddiqui MR, Siddiqui FM, 2012, A man with leonine facies.
pachydermoperiostosis: A case report. Mymensingh Med J, BMJ Case Rep, 2012, bcr1020115057.
26(4): 939–943. https://doi.org/10.1136/bcr.10.2011.5057
87. Mone FH, Roy K, Hasan GZ, et al., Peutz-Jeghars’ syndrome, 99. Khan M, Uzzaman MM, Tasnim S, et al., 2018, Phenotypic
a rare genetic disorder: A case report. J Med Res Health Sci, distribution of turner syndrome in Bangladesh: An analysis
3(7): 1029–1032. of 446 cases phenotypic distribution of turner syndrome in
Bangladesh: An Mansura Khan Mohammad Moniruzzaman
https://doi.org/10.15520/jmrhs.v3i7.221
Sadia Tasnim Zarina Akhter. Int J Sci Res, 7(6): 17-19.
88. Hanif A, Hasina K, Hassan MK, et al., 2010, Two case reports 100. Mahtab H, Akhtaruzzaman M, Rezwan S, 1984, Human
of Peutz Jegher’s syndrome. J Paediatr Surg Bangladesh, 1(1):
77–79. cytogenetical case report of Turner’s syndrome. Report-I.
Bangladesh Med Res Counc Bull, 10(1): 7–12.
https://doi.org/10.3329/jpsb.v1i1.19471
101. Islam F, Afroza A, Rukunuzzaman M, et al., 2008, Treacher
89. Anwar S, Kamal N, Khanom R, et al., 2019, Recurrent Collins Syndrome - A case report. Bangladesh J Child Health,
abdominal pain in Peutz-Jeghers syndrome: A case report. 32(1): 33–36.
J Bangladesh Coll Physicians Surg, 37(3): 160–164.
https://doi.org/10.3329/bjch.v32i1.6011
https://doi.org/10.3329/jbcps.v37i3.41739
102. Rahman A, Islam AM, Husnayen S, 2012, Recurrent deep
90. Sultana S, Hossain ML, Parvin MN, 2020, Pattern and vein thrombosis due to thrombophilia. Korean Circ J,
treatment of Parkinson’s disease at different health care 42(5): 345.
levels in Bangladesh: A hospital based survey. Int J Sci Rep,
6(4): 139. https://doi.org/10.4070/kcj.2012.42.5.345
103. Nahar N, Sultana S, Chowdhury M, et al., 2013, A girl with
https://doi.org/10.18203/issn.2454-2156.IntJSciRep20201269
ulcerative colitis in a tertiary care hospital - A case report.
91. Biswas RS, Khan MH, 2013, A young Bangladeshi male with Pulse, 6(1–2): 53–56.
porphyria cutanea tarda. J Case Rep, 3(2): 259–261.
https://doi.org/10.3329/pulse.v6i1-2.20352
https://doi.org/10.17659/01.2013.0061
104. Choudhury T, Jahan S, Kamal M, et al., 2012, Von Hippel-
92. Chowdhury MK, Chakrabortty R, Gope S, 2015, Poland’s Lindau disease in a pregnant lady. Mymensingh Med J,
syndrome: A case report and review of literature. J Pak Med 21(1): 184–187.
Assoc, 65(1): 87–9.
105. Rashid R, Mazumder MW, Karim AB, et al., 2019, von
93. Hossain HT, Khandaker MA, Islam QT, et al., 2018, Poland Willebrand Disease, A rare cause of massive upper GI
syndrome - A rare congenital condition. J Bangladesh Coll bleeding: A case report. Bangladesh J Child Health, 43(3):
Physicians Surg, 36(4): 166–169. 188–191.
https://doi.org/10.3329/jbcps.v36i4.38186 https://doi.org/10.3329/bjch.v43i3.49581
94. Kibtiar M, Parvin R, Talukder MK, et al., 2019, Spinal 106. Akhter S, Kabir MS, Majumder S, et al., 2016, Wilson disease
muscular atrophy type 3: A case report. Bangladesh J Child in a Bangladeshi child: A case report. Bangladesh Med J,
Health, 43(3): 183–187. 45(1): 54–56.
https://doi.org/10.3329/bjch.v43i3.49580 https://doi.org/10.3329/bmj.v45i1.28969
95. Khan WA, Banu B, Amin S, et al., 2005, Prevalence of Beta 107. Rukunuzzaman M, 2015, Wilson’s disease in Bangladeshi
thalassemia trait and Hb E trait in Bangladeshi school children: Analysis of 100 cases. Pediatr Gastroenterol Hepatol

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