Dr Bushra Afroz's Genetics & Metabolism Clinic, KarachiMedical / Doctor / Pharma service in Eastern Karachi |
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Service DetailsName: Dr Bushra Afroz's Genetics & Metabolism Clinic Type: Medical / Doctor / Pharma Address: Aga Khan University Hospital, Stadium Road, Karachi Description: Consulting Clinic 5: 34861028 Mon 1pm(paktive)-4pm Wed 9am-1pm. Added on Paktive by: Guest From the Paktive Map: East Karachi Services (PECHS, Gulshan, Johar, Korangi, Shahrahe Faisal, Malir and nearby areas.) |
Discuss Dr Bushra Afroz's Genetics & Metabolism Clinic
bushra afroz
Assalam o Allaikum Dear Doctor! today i came to know about your bad health. May Allah Almighty give you health and comfort. I am the father of the baby who is under your kind treatment at agha khan hospital with name Baby Girl of Uzma. Insha Allah we will visit soon for our daughter's check up. i am trying to have an appointment with you but the clinic on last monday was also cancelled and same on tomorrow. At the end i am quite hopeful for your good health. regards M SHAHZAD
My son muhammad ebad ur rehman has 18 month age we want to send u his medical reports, Mam doctor Zohair ali Nanjiani ask me if u dont mind rply plz because i m faraway from karachi (layyah punjab) . Are u visite punjab and where r u visite
My litle cuzen sister hareem naveed is heaving a citeroanemia(metabolic disoder).plz send me your mailing adderes that i can send reports of her to you.kind regards mohsin khurshid
Dear Doctor sb, This is Kashif, son of 4 child, 3 died sons who died at 1.5 years due to hydrocephalous and 1 daughter who is MashAllah good & school going. She also had pyloric stenosis when at 2 months but got operated and fine. Now, i want to have genetic conselling as my wife is my cousin and why my all 3 sons got Hydropcephalous . What can we do ? want to plan baby for daughter/son but much worried. I lives at Lahore but would be at Karachi for 18th and 19th Jan and can visit if get some appointment and contact details. Thanks. Kashif Mahmood
my two months old kid z having interactable sciezers with suspession of neurometabolic disorder .microcephalic HC 31 cm .i hv already lost my two kids with same insult @ the age of 16 and 28 months of age .urin for redicing substtance z positive.TFTs reduced .ABGs normal ..on oral protein free diet .Lerace .Dormicum tds.L carnitin .BiotinSteroid .ACTH 25 uniys bd.phenytoin .but still fits not controlled .so help me in making dx of my child and further strategy .
Hi am working at Aga Khan Foundation Pakistan. My frend's daughter has metabolic disorder with plasma ammonia 84. Can you please provide your contact details so he can contact you as he is in peshawar and doctors are unable to provide treatment to that child. This is his 2nd daughter and his 1st baby was died due to almost same genetic issues. Thanks Ali
Hi its tahira..i lost my 2 sons..dr are saying that they are genetic...1st child had polycystic kidneys and the 2nd was hypotonia,hyperglycimia and many other medical issues...i have given a test of my 2nd son and the reports i have shown to everyone but no one is responsing want to ask u what to do now...i am still hoping...pls reply as soon as i can...wht can i do for the next pregnancy..
I m dailysis patient before 4 years. Weekly 3 time dailysis. Anti HCVpositive during dailysis. I m suffering renal stone dieseas. Doctor said me my family suffring primery oxaluria becuse my stone creat again and again. So posibilitiy kidney and liver both transplant but decieded after test only kidney transplant and kidney liver both transplant. I m alone son of his parents. My parents very disturb for me. My brother expire before 5 years after transplant 5 days. Same problem same condition E mail aneelazubairaneela gmail.com Cell no Whatsup same
mam i dr nadeem working as PGR in children complex multan.mam we want to evaluate patient for biotinidase deficiency.patient is not affording.and we dont know from which lab it is available here in pakistan or abroad..mam you people write an article can you help how this test can be done and from where..we will be thankful
Doctor, i have a problem to discuss with you regarding my friend. His name is Abdul Ahad, he is 21 years of age and is suffering from a disease named Abetalipoproteinemia. His problem is getting worse with age. His younger brother has the same problem but is seemed to be less affected mainly because of his age. From what i see, this problem is in there blood line due to their family inter marriages, as he also tells me that this disease is in there family from 3 generations. doctor is there any way this disease could be treated trough medical surgery/treatment or genetic engineering is the only possible way for the cure of this problem. I need your opinion on this situation. do read my e-mail, your opinion would be really helpful for us to take the next step forward. Thank you for your time and consideration.
I have two baby children one of 9 years age suffering by Herschphrung disease since birth with disability of deaf & dumb and second one is of 6 years age with also disability of speaking Third one was my baby boy who died in Herschphrung disease.Now guide us what should we do now? Much worried about Treatment of my wife me self and my children.Thx .
Mam plz suggest us Some tests Regarding Disability occurs in my Babies since birth which u think best for findings as well as for our treatment of my wife & meself as well. Thx Mam
Doctor UAE meta bolic petant report send pliz soletion pliz pliz
My baby age is 3.5 years and still she is not walking and speaking so doctor suggest for genetic test can you give me the details please
mam Refer by dr shenaz Need to see my patience urgent do inform me when n whear
Mam i have 1 question I have one patient 1year 6 month old presented with complain of respiratory distress nd un able to stand nd walk up to this age. His workup done from aku of inborn eror of metabolism nd simultaneously workup for rickets... His reports showed fumaric aciduria and hypophosphotemic rickets I want to ask is there any relation ship between fumaric hydratase defieciency and hypophophetemic rickets??? Will be thankful to you for ur reply
i have becker muscular dystrophy. no family history. my age is 24. i want to marry but worry about the decease muscular dystrophy that it can pass to my childern or not? please give me answer urgent. thanks
dr shab i am belong from mansehra i want ur email ..my son is musles is weak and i sent u his report .regards
Anabia my 3 and half month child previously alright sudden developed severe vomiting on 10 Feb. On next morning she started excessive crying and gone into respiratory distress On investigation there was metabolic acidosis with hyperammonemia. In northwest General hospital peshawar. Then i took her to pims ialambad .where TMS was send along with plaama amino acid and urine organic acid. Today i recieved TMS report which show Co free carnitine below normal
My 1 year baby had been diagnosed PKU 1 month ago, I m so much worried about him, u m a middle-class man, I can't afford costly PKU milks, could u plz give me some info about cheap products of PKU, Plz give me some PKU affected people's,s cell no so that I can collect info about PKU treatmen. Plz tell me a cheap test of checking phe level in blood,
My 1 year baby had been diagnosed PKU 1 month ago, I m so much worried about him, u m a middle-class man, I can't afford costly PKU milks, could u plz give me some info about cheap products of PKU, Plz give me some PKU affected people's,s cell no so that I can collect info about PKU treatmen. Plz tell me a cheap test of checking phe level in blood,
my daughter was born with homositeinenuria she was diagnosein mount sinai hosptel abroad. She 3 years old.alhumdullia she is doing normel but we still give her b6 b12 and betein .i live in us .i would like to talk with doctor for secound openine i can send u reports too and ur fees thanku so much
@10.Dr.nadeem Qaisrani: we can provide you support for this testing we also provide next generation sequensing test in pakistan for more plz feel free to ask Adnan Shikoh Taimure Center karachi pakistan
@5.Kashif Mahmood: your kid had ammonia issue ? Did he got recover after surgery ? Which surgery ?
I want to consult dr .bushra afroz .I face problems in 6 years.my two babies death produce a big problem to me at the disease of bilary Artesia so plZ I want to help ur experience contact.
@8.Tahira: . Mam i m 5 year marriage. My two child born but not live and death one by one after 6 month. Dr. Says gentic issue because of cousin marriage and spinal muscular atrophy (SMA)diseas.mam advise further.
@27.Aftab Ahmad: mam i am 5 year s marriage.mam after 16 month marriage born child normal delvary but he not move legs and control head.dr says (SMA)spinal muscular atrophy .but my child not live and death 6 month.2nd child born after 16 month but he same position Dr.says(SMA) spinal muscular atrophy and he death 6 month. Mam Dr. Says Genetic issue because of cousin marriage.but i m 2nd cousin marriage.mam please advise me further treatment or soulation PLZ. Thanks I prayer for you till life.
Miss my name is shoaib liaqat. I hve a daughter.2 yrs old.she is patient of metabolic disorder. send me ur email,i will mail u complete history and file of her.i shell be very thankful to u. I am from khanewal and inshallah with ur help and support i will start her treatment. Thankyou
KINDLY, ARRANGE THE NICU AGA KHAN, FOR THIS BABY SHE IS SERIOUSLY ILL, SUGAR DOWN, AFTER 12 HOURS, 18, HOURS, THIS TIME THIS BABY ADMITTED IN ZIAUDDIN HOSPITAL.
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Dr i am hadi ahmed and i have Two Son, one is 5 year old and the 2nd is 4 year around both are CP child. we want to plan for another baby and would like to discuss with you regarding the case. guide us Thanks Regards Hadi ahmed
Mam, my niece is suffering from regression of milestone donor know exact issue. One niece is died two years before she is also not fine I need your contact number so we can discuss it further n need your help. Your contact no or email is required. We lived in Islamabad so I will come after getting confirmation from you Thanks in advance n reply soon.
I need dr bushra afroz appointment. I am from mardan
Dr.i am Sarah..I have 3 children 2 son and one daughter my son are so good and going 2 school bt my daughter is not well she is patient of phynylalanine .she is 2 years old but unable to sitting,standing,walking,and talking.she is still not growing me so worried I live in Multan .Multan Dr says she is inborn of error of metabolism .Dr refer to pku milk bt I cant afford it Dr give me any opinion I am far away from Karachi I have little money bt I cant come to Karachi Dr give me any suggestion I am waiting for ur reply
Madam i am was your patient on date 3 December 2014 in AKU I was with fever of typhoid and was admitted 3 days and was vaccinated but after that typhoid has happened 2 times again yesterday i came for vaccination and met with a general physician he said that you should go to a infection specialist for further treatment
I visited doctor bushra afroz with my kid on 24/09/2018 I just wonder how she become a doctor she is not like a doctor who have zero tolerance to listen she was behaving that she is something special I recommend nobody will visit her and save your money it is useless to consult her when I ask why other doctor recommend me to consult you she says ask the doctor who recommend she think all of the people who visited are dumb and do not know any thing. Me and most of the people who visited doctors already done lot of study about his or her patient and already spend lot of time with the doctors so stop treating people like they are dumb you are taking fees of consultation so behave your self when treat patient and their attendant and give full attention to them.
I want appointment for my baby
Does dr bushra do clinics in any other hospital. Other than aga khan?
My daughter is 2years age suffering from PKU. Her growth is much slow. Kindly advise me a better diet for her treatment. I will be waiting for your kind response as soon as possible. Regards! Osman Hashmi Cell No is
@15.Sameer: Hello. Mr Sameer I think we should talk about this matter. Bcoz I had also 2 children like this.
Rudest doctor ever highly unethical. Worst communicator as a doctor. doesn't matter how qualified she is if she cannot talk politely she is the most illiterate person I've come across.
Dr. I have 2 daughters and both have delayed milestones problem my younger daughters age is 3 me and my wife are planning 3rd baby but we are afraid help us to suggest that what to do???
I lost my two kids One is my 2years daughter and second one is my three days son My daughter have poor immune system she have vomit problem
my son is metabolizam pishent
Dr Bushra Afroz .i am from rawalpindi..my daughter Haniya is methylmalonic acidemia patient.. i need your contact number and appointment procedure..
My son Naveed Muhammad Raffay u suggest for homocysteine test fro USA then i go to Aga kahn lab they replied waiting some days so if u say to lab then we do test early n posible
@42.Anabya Ismael: i want to ask about dr bushra i have lost my 2 kids coz genetics issue plz guide me about her
Please help my baby due to metabolic disorder
@37.Zeeshan: u r absoulty rite i have lost my two kids i viste her highly unethical bad behaviour rudest dr
I live in Lahore. My new born baby has HMG COA lyse deficiency. I want to discuss the case with you give me your contact number. I am very thankful to you.
@46.Tahir Ali Give your contact number
Everyone. metabolic problem babies problem share experience so friends context no share group may add Thanks
i m dr noorunisa assistant professor jsmu.my niece daughters ( 1st baby age 3 months expired 2018 without diagnosis )and 2nd baby diagnosed cystic fibrosis expired 23 November 2019 2 month age.want to meet u for further information
@1.Am: Dr.bushra Afroze birth asphxia Doctors birth bad Brian hospital death reports birth lady Dufferin hospital karachi
Salam dr bushra afroz 5
Dr, age 10 year prroblem he doctors appoint lie advise to appoint
Shughlla is My first doughtier she is 20months old she can not set nor stand.what can I do for her.
Mem, My nephew age 6m diagnose pku (phenylketonuria) some one ask you are the only who treat this kind of patients pls guide and reply . Regards Shabbir Bahawalpur Punjab
beta 8 month metabolic disorder disease diagnose 3 baba or Allah JB m AP s chkup hi.i am too worried
baby 1.30 years he neck he bar bar body head exray he
My daughter is a patient of Dr. Bushra.. she is 5 year old now.. she is a canaven disease patient... We want to do test urine NAA for her.. please inform me whether it is done from outside Pakistan through Agha Khan Hospital Thanks
@50.Sairaamir: agree She is a rudest Dr / Consultant i have meet ever, even sometimes i think
Very poor uneducated money making doctor stupid questions were asked and told us she can not help us at all. Left very disappointed did help us at all did not even look at my child his height and weight. Treated parents and child poorly no help please do not waste your money.
@43.M.haris Khan: consult with Dr. Shabbir Ahmed Malik https://www.paktive.com/Dr-Shabbir-Ahmed-Maliks-Clinic_2843EA03.html Liaquat National Hospital, Karachi just a second opinion
@49.Abdul Basit: What happened baby?
@65.Farhan Sheikh: thanks bro, i followed your advice, and found him the best doctor for metabolic problems
@67.Anwar: please🙏 pray for daughter
My son's test has come but till now you have not replied name Muhammad Maher you told me that you are from kpk we will call ourselves
Details: Muzaffargarh - Address: Punjab - Photo: Muzaffargarh https://www.paktive.com/maps/muzaffargarh.html - Contact: https://www.paktive.com/postalcodes/Muzaffargarh-Punjab.html