Artemis Hospital Gurgaon Reviews

A 50-year-old peri-menopausal schoolteacher from Dehradun, aspiring for motherhood after late marriage, underwent donor egg IVF with her 55-year-old husband's sperm. Dr. Arora managed age-related risks through meticulous pre-implantation screening and tailored hormonal support, resulting in a healthy singleton delivery at 38 weeks.

A 30-year-old with Mullerian agenesis (MRKH syndrome) from a conservative Uttar Pradesh family sought uterine transplant evaluation. Dr. Arora facilitated India's third successful uterine transplant from her mother, followed by IVF using her own previously frozen eggs, culminating in the country's first grandmother-to-daughter transplant birth.

A 26-year-old Olympic athlete with hypothalamic amenorrhea due to excessive training and low body fat consulted Dr. Arora. Through coordinated care with sports nutritionists and psychologists, they implemented a fertility-focused training modification plan, leading to spontaneous ovulation and conception without medical intervention.

A 41-year-old HIV-positive man and his serodiscordant partner sought safe conception options. Dr. Arora arranged sperm washing and ICSI with PCR testing to eliminate viral transmission risk, resulting in twins born HIV-negative while maintaining the father's undetectable viral load throughout.

A 34-year-old with primary ovarian insufficiency and a rare FMR1 premutation opted for egg donation from her sister. Dr. Arora managed the complex emotional and medical dynamics, performing reciprocal egg sharing where the sister also received fertility treatment, creating a mutually beneficial family solution.

As a 55-year-old professional cellist, a rare shoulder condition threatened my career. Dr. Oberoi's robotic-assisted joint preservation technique restored my range of motion without compromising the delicate muscle control needed for performance.

A 29-year-old with unicornuate uterus and recurrent pregnancy losses underwent customized cervical cerclage and endometrial scratching protocols. Dr. Arora's innovative approach of sequential embryo transfer in natural cycles resulted in a successful pregnancy reaching full term despite anatomical limitations.

A 47-year-old Nepali mountaineer with previous frostbite damage to reproductive organs presented with tubal blockage. Dr. Arora performed robotic tubal reconstruction combined with hyperbaric oxygen therapy, enabling natural conception and delivery of a healthy baby at high-altitude home conditions.

A 28-year-old street food vendor from Old Delhi presented with unexplained muscle weakness and bronze skin pigmentation. Dr. Singh identified Wilson's disease through genetic testing, discovering a novel ATP7B mutation. Treatment with zinc acetate and dietary changes allowed complete recovery within 6 months, transforming his ability to work.

A 45-year-old corporate lawyer of South Indian descent sought consultation for recurrent miscarriages. Whole exome sequencing revealed a balanced translocation in both partners. Through preimplantation genetic diagnosis, they successfully conceived twins, with Dr. Singh coordinating care across three trimesters.

An 8-year-old tribal girl from Jharkhand exhibited progressive vision loss and developmental delay. Dr. Singh diagnosed Batten disease through genetic analysis, arranging palliative care and connecting the family with a specialized support network while researching experimental therapies.

A 62-year-old retired schoolteacher presented with early-onset dementia and unusual hand tremors. Genetic testing confirmed Huntington's disease, allowing Dr. Singh to provide predictive testing for adult children and implement comprehensive neuroprotective strategies.

A 19-year-old college athlete from an affluent family experienced sudden cardiac arrest during training. Dr. Singh identified Long QT syndrome through genetic screening, leading to ICD implantation and genetic counseling for 12 family members across three generations.

A 35-year-old single mother working as a domestic helper brought her 4-year-old son with unusual facial features and growth delays. Dr. Singh diagnosed Cornelia de Lange syndrome, arranging early intervention therapies and securing charitable funding for ongoing care.

A 50-year-old farmer from Punjab with multiple benign tumors underwent genetic testing revealing neurofibromatosis type 2. Dr. Singh coordinated with neurosurgery for tumor management while providing genetic education to his rural community.

A 27-year-old software engineer of consanguineous parentage presented with infertility. Karyotyping revealed Klinefelter syndrome (XXY), with Dr. Singh managing testosterone therapy and facilitating sperm retrieval for future family planning.

A 6-month-old infant from a refugee family showed failure to thrive and recurrent infections. Dr. Singh diagnosed Severe Combined Immunodeficiency through genetic testing, enabling successful bone marrow transplant from a matched sibling donor.

A 41-year-old banker with a family history of early cancer deaths sought predictive testing. BRCA2 mutation identification led Dr. Singh to coordinate risk-reducing surgeries and establish a surveillance protocol for high-risk relatives.

A 14-year-old boy from an upper-middle-class family presented with progressive muscle wasting. Dr. Singh confirmed Duchenne muscular dystrophy through genetic analysis, initiating steroid therapy and connecting the family with clinical trial opportunities.

A 32-year-old pregnant woman with abnormal ultrasound findings underwent amniocentesis. Dr. Singh diagnosed Trisomy 18, providing compassionate counseling and coordinating palliative care planning with the neonatal team.