Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Zahoor Hussain Daraz"'
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 10, Iss 2 (2017)
Hutchinson-Gilford progeria syndrome (HGPS) is a rare genetic disease in which symptoms of aging are manifested at an early age. In the present report, we describe a 9 months old female child presented with a history of progressive coarsening of skin
Externí odkaz:
https://doaj.org/article/d4dea6fbdc634ab998ea4cc01d84dcc8
Autor:
Mohammed Mahbubul Islam, Mujammel Haque, Zahoor Hussain Daraz, Sufia Khatun Sumi, Mohammad Imnul Islam, Shahana A. Rahman
Publikováno v:
Bangabandhu Sheikh Mujib Medical University Journal, Vol 9, Iss 2 (2016)
Larsen syndrome is a rare inherited disorder characterized by congenital dislocation of multiple joints along with other anomalies of heart, face, hands and bones. Larsen syndrome was first described in 1950 by Larsen, Schottstaedt and Bost. In the p
Externí odkaz:
https://doaj.org/article/373bba8695f44417abf2955fe0f18793
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. :146-149
Objective: The goal of our study was to determine the magnitude, prevalence and severity of iron deficiency anemia among children in Doda (J&K) India. Methods: It was a prospective, cross-sectional, multistage hospital-based and outpatient department
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2119668b91be45dee733e131e4d80947
https://doi.org/10.22159/ajpcr.2023.v16i1.46239
https://doi.org/10.22159/ajpcr.2023.v16i1.46239
Publikováno v:
International Journal of Science and Healthcare Research. 7:46-48
WHO defines health inequities as avoidable inequalities between groups of people within countries and between the countries: Similarly, various global health agencies have provided an extract where Inequity and inequality is clearly defined. These tw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::283a9192216452a9eb4aff8b22ca5b0a
https://doi.org/10.52403/ijshr.20220109
https://doi.org/10.52403/ijshr.20220109
Publikováno v:
International Journal of Science and Healthcare Research. 6:348-350
Canavan disease is a rare autosomal recessive disorder characterized by progressive leukodystrophy involving white matter of the brain. Disease leads to severe psychomotor retardation, seizures and premature death. More prevalent among Jewish populat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ead308b4bae4214450f9d67cd8355a2e
https://doi.org/10.52403/ijshr.20211048
https://doi.org/10.52403/ijshr.20211048
Autor:
Mortuza Begum Mortuza Begum, Md. Sanaullah Shelly Md. Sanaullah Shelly, Zahoor Hussain Daraz, Adnan Bacha, Berkheez Shabir
Publikováno v:
World Journal of Current Medical and Pharmaceutical Research. :224-227
We report a case of recurrent mucinous carcinoma of the breast in a 60 year old female who presented with two separate lumps on the left chest wall for 1 year. She gave the history of left sided mastectomy 15 years ago and hysterectomy 10 years ago.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5fd832641cb1c2ee8da1c3ec83e082cb
https://doi.org/10.37022/wjcmpr.vi.134
https://doi.org/10.37022/wjcmpr.vi.134
Publikováno v:
Journal of Bangladesh College of Physicians and Surgeons. 38:101-104
Primary complement deficiencies are very rare and a case of 6 year old girl with complement 3 deficiency is reported here who presented with recurrent infections and rash since her early childhood. She had several episodes of respiratory tract infect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09cc4ab0ad959366fe8b6b67a91db248
https://doi.org/10.3329/jbcps.v38i2.45636
https://doi.org/10.3329/jbcps.v38i2.45636
Autor:
Zahoor Hussain Daraz, Berkheez Shabir
Publikováno v:
World Journal of Current Medical and Pharmaceutical Research. :178-180
The incidence of placenta accreta spectrum (PAS) disorders has increased over the last decades due to increase in cesarean deliveries, resulting in increase in cesarean hysterectomies , maternal mortality and morbidity but since last few years there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f9c77bf3d844bdba11851c191d8a242
https://doi.org/10.37022/wjcmpr.2020.2217
https://doi.org/10.37022/wjcmpr.2020.2217
Publikováno v:
World Journal of Current Medical and Pharmaceutical Research. :139-141
In 2019, an outbreak of hand, foot and mouth disease (HFMD)occurred in Maldives and many patients presented with onychomadesis following HFMD. Here we present a study of 33 cases out of which a total of 06 cases developed onychomadesis. Patients vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72b872a667f2e27b5d0f9db52867d522
https://doi.org/10.37022/wjcmpr.2020.2209
https://doi.org/10.37022/wjcmpr.2020.2209
Autor:
Mohamed Rashwan Meselhy shady, Pramesh Kumar Yadav, Rehana Afshan, Berkheez Shabir, Zahoor Hussain Daraz
Publikováno v:
World Journal of Current Medical and Pharmaceutical Research. :79-80
A 3-year-old boy presented to our atoll hospital in H.A Alif Dhidhoo, with severe pallor, jaundice, easy fatigability and recurrent episodes of passage of dark-colored urine for past 3 days. He was born mature at 39 weeks of gestation with no past si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78ff94aa38a883d29c331059ac2046fc
https://doi.org/10.37022/wjcmpr.v3i4.179
https://doi.org/10.37022/wjcmpr.v3i4.179