Dr. Singanamalla Bhanudeep
Consultant Pediatric Neurologist
MBBS, MD Pediatrics (JIPMER), DM Pediatric Neurology (PGIMER)
8+ years Experience
Madinaguda, Kukatpally
English, Telugu, Hindi, Tamil
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About Dr. Singanamalla Bhanudeep
Dr. Singanamalla Bhanudeep is a dedicated Pediatric Neurologist with over 8 years of clinical experience. Dr. Bhanudeep has done an MBBS from Andhra Medical College, Visakhapatnam, and an MD (Pediatrics) from Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER), Puducherry. He did a DM in Pediatric Neurology from the famous Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh, where he was trained in diagnosing and treating a variety of neurological disorders in infants, children and adolescents.
Dr. Bhanudeep has vast experience in management of Epilepsy, Developmental disorders, Neuromuscular diseases, Neurogenetic disorders, Autoimmune neurological disorders and Acute neurological emergencies. He is experienced in pediatric neurophysiology including EEG, EMG, NCV, VEP and BERA studies.
Dr. Bhanudeep is committed to compassionate and evidence-based treatment. He strongly believes that early diagnosis, appropriate intervention and multidisciplinary rehabilitation are the key factors to help children reach their maximum developmental potential. He works with families to provide comprehensive neurological care and improve the long-term health and quality of life of his patients through a patient-centered approach.
Dr. Singanamalla Bhanudeep is a Consultant Pediatric Neurologist and practices at Ankura Hospital for Women and Children, Madinaguda and Kukatpally.
Field Of Expertise
Pediatric epilepsy and seizure disorders.
Early infantile epilepsy.
Refractory and super-refractory seizures.
Febrile seizures and febrile encephalopathy.
Autism Spectrum Disorder (ASD).
Developmental delay and neurodevelopmental disorders.
Neuromuscular disorders.
Neurogenetic and neurometabolic disorders.
Autoimmune neurological disorders.
Pediatric headache disorders.
EEG, long-term video EEG monitoring.
EMG, NCV, VEP and BERA studies.
Neurorehabilitation.
Pediatric neurological emergencies.
Research & Publications
Dr. Singanamalla Bhanudeep has made significant academic contributions to the field of Pediatric Neurology through extensive research and scholarly publications in leading national and international peer-reviewed journals. His work focuses on epilepsy, infantile spasms (West syndrome), neurometabolic disorders, neurogenetics, developmental epileptic encephalopathies, neuromuscular disorders, neuroimaging, rare neurological diseases, and pediatric neurocritical care.
Over the course of his academic career, Dr. Bhanudeep has authored and co-authored 96 peer-reviewed scientific publications in reputed journals, which include the following:
1. Kiruba Samuel EM, Krishnamurthy S, Bhanudeep S, Muske S. Levamisole in Frequently-relapsing and Steroid-dependent Nephrotic Syndrome. Indian Pediatr. 2017; 54:831-834.
2. Kathiravan M, Dhawan SR, Singanamala B, Saini L, Sahu JK. Levetiracetam Induced Neuropsychiatric Manifestation in a 5-year-old Boy. Indian J Pediatr. 2019; 86:193.
3. Dhawan SR, Adhikari U, Singanamala B, Kumaran S, Saini AG, Saini L. Recurrent Cerebrospinal Fluid Pleocytosis. Indian J Pediatr. 2019; 86:308–309.
4. Singanamalla B, Kesavan S, Saini AG. Familial Spastic Paraparesis: A Novel Mutation in a 4-Year-Old Girl. Ann Indian Acad Neurol. 2020; 23:386-387.
5. Madaan P, Singanamala B, Saini L. Diagnostic Clue in Repetitive Hand Movements. Pediatr Neurol. 2019; 101:88.
6. Randhawa M, Dhawan SR, Kumar S, Singanamala B et al. Wormian Bones and Dilated Scalp Veins in an Infant With Epilepsy. J Pediatr Neurosci. 2019; 14:103–104.
7. Saini S, Singanamala B, Saini AG. Intellectual disability in boys: mark the face!. BMJ Case Rep. 2019;12: e229271.
8. Singanamalla B, Saini AG, Sidana V, Saini L, Sankhyan N, Singh P. Progressive quadriparesis and inflammation: A common disease, a rare presentation. Indian J Tuberc. 2020;67:336-339.
9. Singanamala B, Noolu R, Madaan P, Saini L. Rhythmic Tongue Thrusting: A Useful Clinical Sign. Pediatr Neurol. 2020; 102:81–82.
10. Singanamalla B, Suthar R. Rhythmic Head Nodding With Absence Seizures. Pediatr Neurol. 2020; 102:78.
11. Singanamalla B, Singh B, Saini L, Ahuja CK, Verma S, Madaan P, Sankhyan N. Disseminated Cysticercosis-A Tropical Curse. J Pediatr. 2020; 217:213.
12. Singanamalla B, Saini AG, Sankhyan N. Exaggerated Startle and Cherry-Red Spots: Important Bedside Clues. Pediatr Neurol. 2020; 105:73-74.
13. Sharawat IK, Saini L, Singanamala B, Saini AG, Sahu JK, Attri SV, Sankhyan N. Metabolic crisis after trivial head trauma in late-onset isolated sulfite oxidase deficiency: Report of two new cases and review of published patients. Brain Dev. 2020; 42:157-164.
14. Singanamala B, Saini L, Madaan P, Singh P, Vaidya PC, Sahu JK. Antitubercular therapy-induced psychosis. Neurology. 2019; 93:1012–1013.
15. Singanamalla B, Mohandoss V, Suthar R, Ahuja CK, Sahu JK. Marcus Gunn Jaw Winking Phenomenon with Cortical Malformation. Indian J Pediatr. 2020; 87:466-467.
16. Reddy C, Singanamala B, Madaan P, Saini L, Sankhyan N. Oculomotor apraxia: a useful clinical sign. Indian Journal of Paediatric Neurology 2020; in press
17. Singanamalla B, Singh AK, Saini AG. Progressive EEG Changes in CDKL-5 Related Epileptic Encephalopathy. Indian J Pediatr. 2020; 87:235-236.
18. Singanamalla B, Dhawan S, Saini AG, Singh P, Sankhyan N. Black Holes in the Brain and Spine: A Dark Disease. J Pediatr Neurosci. 2020; 15:63-64.
19. Singanamalla B, Madaan P, Saini L, Sankhyan N. Vitamin B12 Deficiency: An Association or Etiology of Pseudotumor Cerebri in An Infant. Indian J Pediatr. 2020; 87:658-659.
20. Madaan P, Singanamalla B, Saini L. Conventional Teaching: Classical Clues. Indian J Pediatr. 2020.
21. Bhanudeep S, Madaan P, Bharadwaj N, Saini L, De D. West Syndrome and Neurocutaneous Syndromes: A Never-ending Association. J Pediatr Neurosci. 2020; 15:162-163.
22. Kesavan S, Singanamalla B, Krishna Sahitya DS, Saini AG, Vyas S. Epilepsy and Hydrocephalus: Should Pyridoxine-Dependent Epilepsy Cross Our Minds?. Ann Indian Acad Neurol. 2020; 23:239-241.
23. Jogu SS, Singanamalla B, Madaan P, Sharma A, Saini L. Kluver-Bucy syndrome: A rare aftermath of tubercular meningitis. Indian J Tuberc. Article in Press doi:10.1016/j.ijtb.2020.08.008
24. Singanamalla B, Babbar A, Tenzin P, Kesavan S, Madaan P, Saini L. Unmasking the Masquerader: A Life Changing Therapeutic Trial. Indian J Pediatr. 2020;87:956.
25. Kaur J, Singanamalla B, Suresh RG, Saini AG. Insensitivity to Pain, Self-mutilation, and Neuropathy Associated With PRDM12. Pediatr Neurol. 2020;110:95-96.
26. Singanamalla B, Madaan P, Saini L. COVID-19 Pandemic and Child Neurology Training: A Bumpy Road Ahead. Pediatr Neurol. 2020:S0887-8994(20)30331-3.
27. Singanamalla B, Chaurasia S, Jain C, Bhatia V, Sharma N, Madaan P et al. Horizontal Gaze Palsy, Scoliosis, and Split Pons Sign in a 6-Year-Old Girl. J Neuroophthalmol.2020.
28. Madaan P, Singanamalla B, Saini L. Neurological manifestations of COVID-19 in children: Time to be more vigilant. Pediatr Neurol. 2020;S0887899420303635.
29. Singanamalla B, Saini L. Diagnostic gait pattern in a treatable neuromuscular disorder. Indian J Med Res. 2020;152(Suppl 1):S82.
30. Singanamalla B, Bhagwat C, Madaan P, Saini L, De D. Forehead plaque in a child with epilepsy: A clue for tuberous sclerosis. Trop Doct. 2020:49475520972523.
31. Singanamalla B, Madaan P, Saini L. Acute Flaccid Myelitis surveillance amidst COVID-19 pandemic. Pediatr Neurol. 2020.
32. Singanamalla B, Madaan P, Saini L, Sankhyan N. Child with predominant midline stereotypies and infrequent seizures. BMJ Case Rep. 2021;14:e238764.
33. Singanamalla B, Paria P, Gunasekaran PK, Saini AG. GAD65-Related Immune Epilepsy: Are we Looking Yet? Indian J Pediatr. 2021.
34. Reddy C, Paria P, Bhanudeep S, Bhatia V, Saini AG. PCDH12-Related Movement Disorder. J Pediatr Neurol. 2021;s-0040-1722619.
35. Reddy C, Paria P, Chatterjee D, Saini AG, Suthar R, Singanamalla B, et al. Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1): Are We Diagnosing Yet? J Pediatr Neurol. 2021;s-0040-1721800.
36. Kumar S, Kumar V, Singanamalla B, Vyas S, Angurana S. Acute necrotizing encephalopathy of childhood: Not always devastating. J Pediatr Crit Care. 2021;8:47.
37. Bhanudeep S, Madaan P, Saini A, Vyas S, Saini L. Florid Brain Calcification in a Child with X-Linked Adrenoleukodystrophy: What Does it Signify? Ann Indian Acad Neurol. 2021. Ahead of Print
38. Singanamalla B, Saini A, Attri S, Suthar R, Mukhopadhyay K. Carbonic Anhydrase-VA Deficiency: A Close Mimicker of Urea Cycle Disorders. Ann Indian Acad Neurol. 2021.Ahead of Print
39. Bhanudeep S, Madaan P, Sankhyan N, Saini L, Malhi P, Suthar R, et al. Long-term epilepsy control, motor function, cognition, sleep and quality of life in children with West syndrome. Epilepsy Res. 2021;173:106629.
40. Bhanudeep S, Rameshkumar R, Chidambaram M, Selvan T, Mahadevan S. Prospective Inverse Probability of Treatment-Weighting Analysis of the Clinical Outcome of Red
Blood Cell Transfusion Practice in Critically Ill Children. Indian J Pediatr. 2021. Ahead of Print
41. Singanamalla B, Vyas S, Madaan P. et al. Ptosis, Visual Blurring, and Multiple Cranial Nerve Tumors: Do We Know the Culprit. Indian J Otolaryngol Head Neck Surg.2021 (Ahead of Print)
42. Singanamalla B, Bhagwat C, Madaan P, Saini L, Srivastava P. Monozygotic twins with development delay and a characteristic electroencephalographic pattern: Just look at the face. J Paediatr Child Health. 2021 (Ahead of print)
43. Raithatha D, Sahu JK, Bhanudeep S et al. Financial Burden in Families of Children with West Syndrome. Indian J Pediatr. 2021 (Ahead of Print)
44. Singanamalla B, Bhagwat C, Madaan P et al. An Infant with Motor Delay and Deafness Due to Usher Syndrome. Indian J Pediatr. 2021 (Ahead of print)
45. Bhanudeep S, Madaan P, Yadav J, Saini L. Pediatric specialty and superspecialty training amid coronavirus disease 2019 pandemic: A thought to ponder. Karnataka Pediatr J 2021;36:60-1
46. Madaan P, Bhanudeep S, Saini L. Status dystonicus in children: Treat the precipitating factors. Karnataka Pediatr J 2021;36:54-6.
47. Rameshkumar R, Chidambaram M, Bhanudeep S et al. Prospective Cohort Study on Cumulative Fluid Balance and Outcome in Critically Ill Children Using a Restrictive Fluid Protocol. Indian J Pediatr. 2021 (Ahead of Print).
48. Jogu SS, Singanamalla B, Madaan P, Ahuja CK, Saini L. Thick corpus callosum: An underrecognised but important diagnostic clue. Trop Doct. 2021 (Ahead of Print).
49. Hassan I, Bhanudeep S, Madaan P, Chhajed M, Saini L. Bilateral calf hypertrophy and isolated motor delay: think beyond muscular dystrophy. J Pediatr Neurosci . (Ahead of Print)
50. Kariyappa V, Singanamalla B, Chaurasia S, Madaan P, Saini L, Vyas S. Developmental delay, vision impairment, and the “double-ring sign.” Indian J Ophthalmol - Case Rep. 2021;1:465.
51. Singanamalla B, Kesavan S, Aggarwal D et al. Marked Facial Weakness, Ptosis, and Hanging Jaw: A Case with RYR1-Related Congenital Centronuclear Myopathy. J Pediatr Genet.(Ahead of print)
52. Singanamalla B, Kochar G, Saini A. Oculogyric crisis in a girl with infantile parkinsonism-dystonia-2. Ann Indian Acad Neurol. 2021.Ahead of Print
53. Chauhan A, Sahu JK, Singh M, Jaiswal N, Agarwal A, Bhanudeep S, Pradhan P, Singh M. Burden of Attention Deficit Hyperactivity Disorder (ADHD) in Indian Children: A Systematic Review and Meta-Analysis. Indian J Pediatr. 2022. (Ahead of print)
54. Singanamalla B, Natarajan R, Madaan P, Saini L. Role of genotype–phenotype correlation in prognostication of a child with a novel potassium channelopathy. J Pediatr Neurosci [Epub ahead of print]
55. Banga V, Singanamalla B, Saini L. Infantile-onset myasthenia: Is it always congenital?. Indian J Ophthalmol Case Rep 2022; (Ahead of Print)
56. Singanamalla B, Paria P, Suthar R, Saini AG, Attri SV. The Challenge of Severe Acute Malnutrition in Inborn Errors of Metabolism: Does Medical Food Alone Suffice? J Pediatr Genet.(Ahead of print)
57. Kaur J, Bhanudeep S, Suresh RG, Saini AG, Bhatia V. Neurodegeneration with progressive dystonia: Juvenile-onset tay–Sachs disease. Ann Indian Acad Neurol. 2022.Ahead of Print
58. Chhajed M, Gunasekaran PK, Bhanudeep S, Saini L. Charcot-Marie-Tooth Disease Type 4C and Autosomal Dominant Heterozygous Ichthyosis Vulgaris, with Bilateral Hearing Loss: A Novel Association with Review of Literature. J Pediatr Genet.(Ahead of print)
59. Makam L, Saini L, Bhanudeep S, Verma S, Madaan P, Verma R, Singh P. Recurrent Pyogenic Meningitis: Never Ever Idiopathic. Neurol India 2022;70:2319-20
60. Bhanudeep S, Bhargavi B, Reddy S. A Clinico-Radiologic Mimicker of Dystroglycanopathies and Congenital Cytomegalovirus Infection. Neurol India 2023;71:151-2
61. Reddy C, Vyas S, Bhanudeep S, Bhagwat C et al. ‘Leukodystrophy’ Like Variant of a Treatable Demyelinating Disorder. Journal of Pediatric Neurosciences 18:p 179-180, April-June 2023
62. Saini AG, Singanamalla B, Gunasekaran PK, Didwal G, Attri SV. Knowledge and experiences of healthcare workers in managing children with neurometabolic disorders in a developing country: a cross-sectional study. J Trop Pediatr. 2023;69:fmad023.
63. Bhanudeep S, Koneti BB. LEUDEN Syndrome: A Novel Hypomyelinating Leukoencephalopathy in a 1-Year-Old Girl. Ann Indian Acad Neurol. 2024.
64. Singanamalla B, Gunasekaran PK, Saini AG. Facial dysmorphism and Limb abnormalities of Fetal Valproate Syndrome, QJM: An International Journal of Medicine, 2024;, hcae165
65. Bhanudeep S, Koneti BB. SLC39A14 Deficiency: A Rare Cause of Treatable Infantile Neuroregression. Annals of Indian Academy of Neurology:10.4103/aian.aian_571_24, October 04, 2024.
66. Singanamalla B, Koneti BB. Postnatal Severe Chikungunya Encephalopathy in a Neonate. Neurology. 2024;103:e210007.
67. Bhanudeep S, Koneti BB. Successful Management of Acute Necrotizing Encephalopathy in a Child. Indian J Pediatr. 2024 Oct 25.
68. Bhanudeep S, Koneti BB. Episodic Dystonia in an Infant with Spastic Paraplegia Type 11. Indian J Pediatr. 2024 Oct 30.
69. Bhanudeep S, Koneti BB. Childhood Chronic Progressive Ataxia with Normal Neuroimaging: Think of CONDSIAS. Neurol India. 2024.
70. Bhanudeep S, Koneti BB. Pathognomonic Neuroimaging in MEGDEL Syndrome. Indian J Pediatr. 2024 Dec 20.
71. Bhargavi Koneti B, Singanamalla B. Large Nevus Sebaceous in a Newborn: Consider the Brain. Neurology. 2025;104:e210266.
72. Bhanudeep S, Koneti BB. Familial cerebral cavernous malformations in a child with KRIT1 gene. QJM. 2024:hcae250.
73. Bhanudeep S, Koneti BB. Recurrent basal ganglia stroke due to mineralizing lenticulostriate vasculopathy. QJM. 2025:hcaf009
74. Saini AG, Gunasekaran PK, Bhanudeep S, Sharawat IK, Singhi P. Patterns of Use of Complementary, Alternative, and Integrative Medicine in Children with Cerebral Palsy in a Developing Country: A Cross-Sectional Study. Altern Ther Health Med. 2025:AT11354. Epub ahead of print. PMID: 39899550.
75. Singanamalla B, Koneti BB. Unilateral postaxial oligodactyly. BMJ Case Reports CP 2025;18:e264215
76. Koneti BB, Bhanudeep S. Neurofibromatosis type 1 and Hemimegalencephaly: A Rare Association. International Journal of Epilepsy DOI: 10.1055/s-0045-1802981
77. Bhanudeep S, Koneti BB. VPS51-Related Disorder in a Toddler: A Novel Golgipathy. Neurol India. 2025;73:402–3.
78. Singanamalla B, Koneti BB. Large scalp congenital arteriovenous malformation in an infant. BMJ Case Rep. 2025;18:e265733.
79. Katoch D, Singanamalla B, Bhatia V, Saini AG. Teaching NeuroImage: Chorioretinal Atrophy and Neuroimaging Findings in Boucher-Neuhauser Syndrome. Neurology;104:e213728.
80. Bhanudeep, S., Koneti, B.B. A Novel Gene (UFSP2) Associated with Infantile Epileptic Spasms Syndrome. Indian J Pediatr (2025).
81. Bhanudeep, S., Koneti, B.B. Diagnosis of Ataxia in a 2-year-old. Indian J Pediatr (2025).
82. Bhanudeep, S., Koneti, B.B. GJC2-Related Hypomyelination Disorder with Pontine Sparing in an Infant. Indian J Pediatr (2025).
83. Bhanudeep S, Koneti BB. Tetrapolydactyly and Hydrocolpos in an Infant: Neuroimaging Gives Clue to the Diagnosis. Ann Indian Acad Neurol. 2025.
84. Bhanudeep S, Koneti BB. Joubert-Plus Syndrome in an Infant. Neurol India. 2025
85. Bhanudeep S, Koneti BB. SON-Related Syndrome: A Nuclear Speckleopathy. Neurol India. 2025
86. Bhanudeep, S., Koneti, B.B. & Guda, S.P.R. Pyridoxine-Dependent Epilepsy Mimicking as Congenital Muscular Dystrophy. Indian J Pediatr (2025).
87. Bhanudeep, S., Koneti, B.B. Hereditary Hyperekplexia Presenting with Muscle Stiffness, Seizures and Recurrent Apneas in An Infant. Indian J Pediatr (2025).
88. Bhanudeep, S., Koneti, B.B. Unilateral Hemispheric Acute Hemorrhagic Leukoencephalitis in a Surviving Neonate. Indian J Pediatr (2025).
89. Bhanudeep S, Reddy R. Neonatal X-linked recessive chondrodysplasia punctata. QJM. 2025 Oct 31:hcaf268.
90. Bhanudeep S, Koneti BB. Variability in MRI patterns of childhood cerebral adrenoleukodystrophy: A sibling triad case study. QJM. 2025 Nov 26:hcaf297.
91. Bhanudeep S, Ryakala B. Reflex Bathing Epilepsy in a Boy with UPF3B-Related Disorder. Ann Indian Acad Neurol. 2026 Jan 22. doi: 10.4103/aian.aian_1049_25. Epub ahead of print.
92. Bhanudeep S, Karanam S. Asymmetric Trilaminar Sign in a Child with Severe Cytokine Storm Due to Dengue-Associated Acute Necrotizing Encephalopathy of Childhood. Indian J Pediatr. 2026 Feb 2.
93. Bhanudeep S, Koneti BB. Extensive Diffusion Restriction of White Matter, Midbrain, and Basal ganglia in a Neonate with Refractory Hypoglycemic Seizures. Neurol India. 2026;74:555-556.
94. Bhanudeep S, Koneti BB. CHD2-Related Developmental Epileptic Encephalopathy and Angelman Syndrome in a Girl: A Double Jeopardy. Neurol India. 2026 May 1;74(3):552-554.
95. Bhanudeep, S. Asymmetric Trilaminar Sign in a Child with Severe Cytokine Storm Due to Dengue-Associated Acute Necrotizing Encephalopathy of Childhood: Author’s Reply.Indian J Pediatr (2026).
96. Bhanudeep S, Koneti BB. Atypical Neuroimaging and Lateralized Periodic Discharges Plus in a Noncritically Ill Child with Posterior Reversible Encephalopathy Syndrome. Ann Indian Acad Neurol. 2026:10.4103/aian.aian_23_26, May 26, 2026.
Certification & Memberships
MBBS – Andhra Medical College, Visakhapatnam.
MD (Pediatrics) – Jawaharlal Institute of Postgraduate Medical Education & Research (JIPMER), Puducherry.
DM (Pediatric Neurology) – Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh.
Neonatal Advanced Life Support (NALS) Provider – Indian Academy of Pediatrics (IAP).
Pediatric Advanced Life Support (PALS) Provider – Indian Academy of Pediatrics (IAP).
KSCH EEG Course – Lady Hardinge Medical College, New Delhi.
Member – International Child Neurology Association (ICNA).
Member – Indian Academy of Neurology (IAN).
Member – Indian Academy of Pediatrics (IAP).
Member – Association of Child Neurology (AOCN).
Member – Academy of Pediatric Neurology (AOPN).
Member – Indian Epilepsy Society (IES).