A unified "Medical Home" for rare conditions. We combine advanced genomic insights with compassionate, multi-specialty rehabilitation.
Genetic diseases like Down Syndrome, Williams Syndrome, or Prader-Willi syndrome are a guide, not a destination. At Udaan, we specialize in "Syndromic Surveillance"—proactively managing the cardiac and developmental aspects of genetic variations.
Expert assessment to correlate physical features with genetic markers for precise testing selection.
Monitoring biochemical pathways to manage syndromes with nutritional or metabolic components.
Specialized therapy for hypotonia and ligament laxity common in many syndromic profiles.
Identifying unique learning strengths to create customized academic and vocational plans.
Children with genetic disorders do not develop according to standard growth charts. We use special tracking methods (such as Down syndrome charts) to ensure optimal endocrine health.
A deep clinical review to select appropriate testing (Karyotype, CMA, or Exome) based on the child's phenotype.
Baseline cardiac, hearing, and vision checks tailored to the specific risks associated with the identified syndrome.
Multi-specialty therapy goals designed to maximize the child's physical, communicative, and social potential.
2A Om Apartment, Opp. Royal Enfield Showroom, Bariatu-Booty Road, Ranchi, Jharkhand
Coming Soon:- Cheshire Home Road, Opp. Mangalam Banquet Hall, Ranchi
neurodev_ped@gmail.com
+91 9229600627
06513198556
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