- Medical School - All India Institute of Medical Sciences, India (2003-2008)
- Residency - Miami Children's Hospital (2010-2013), Pediatrics
- Fellowship - UT Southwestern/Children's Medical Center (2013-2016), Pediatric Endocrinology
Biography
Dr. Nivedita Patni received her medical degree from All-India Institute of Medical Sciences in India, and completed her pediatric residency at Miami Children’s Hospital before coming to UT Southwestern Medical Center for Pediatric Endocrinology fellowship. Her research interests are focused towards lipodystrophy and genetic dyslipidemias. She has described a novel syndrome of generalized lipodystrophy associated with pilocytic astrocytoma, which was recently published in Journal of Clinical Endocrinology and Metabolism. She continues her research work at the Center for Human Nutrition at UT Southwestern Medical Center to determine the etiology of this syndrome. She is also working on determining genetic basis of lipid disorders in children and investigating the genotype-phenotype relationships in these patients. She designed a study to determine Genetic Bases of type 1 hyperlipoproteinemia (T1HLP) and received a Service Package Grant from the Center for Translational Medicine at UTSW Medical Center, Dallas, Texas. She is also spearheading a clinical trial to evaluate the Efficacy of Orlistat for the Treatment of T1HLP.
Education & Training
Professional Associations & Affiliations
- American Diabetes Association (2015)
- The Pediatric Endocrine Society (2014)
- Pediatric Endocrinologists of Texas, Oklahoma, Louisiana, and Arkansas (2013)
- American Academy of Pediatrics (2010)
- The Endocrine Society (2013)
Honors & Awards
- Travel Award for Lipodystrophy meeting: Leptin and Beyond 2014
- Endocrine Society Early Career Forum Travel Award for Annual Meeting 2015
- Pediatric Endocrine Society Travel Award for Annual Meeting 2016
- Pediatric Endocrine Society Travel Award for Lipodystrophy Diagnosis & Treatment Consensus Statement meeting, 2015
Books & Publications
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Books
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Genetics and Dyslipidemia in Diagnosis and Treatment of Lipid Disorders in Children and Adolescents in www.endotext.org.
Patni N, Ahmad Z, Wilson D. (2016), South Dartmouth: MDText.com, Inc. -
Cerebrotendinous Xanthomatosis in Diagnosis and Treatment of Lipid Disorders in Children and Adolescents in www.endotext.org.
Patni N, Wilson D. (2016), South Dartmouth: MDText.com, Inc.
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Genetics and Dyslipidemia in Diagnosis and Treatment of Lipid Disorders in Children and Adolescents in www.endotext.org.
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Publications
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Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.
Wambach JA, Wegner DJ, Patni N, Kircher M, Willing MC, Baldridge D, Xing C, Agarwal AK, Vergano SAS, Patel C, Grange DK, Kenney A, Najaf T, Nickerson DA, Bamshad MJ, Cole FS, Garg A American journal of human genetics 2018 Dec 103 6 968-975 -
Should children with chronic diarrhea be referred to a lipid clinic?
Wilson DP, Patni N Journal of clinical lipidology 2018 Jun -
Orlistat Therapy for Children with Type 1 Hyperlipoproteinemia: A Randomized Clinical Trial.
Patni N, Quittner C, Garg A The Journal of clinical endocrinology and metabolism 2018 Apr -
The prevalence and etiology of extreme hypertriglyceridemia in children: Data from a tertiary children's hospital.
Patni N, Li X, Adams-Huet B, Garg A Journal of clinical lipidology 2018 Jan -
A Novel Generalized Lipodystrophy-associated Progeroid Syndrome due to recurrent heterozygous LMNA p.T10I Mutation.
Hussain I, Patni N, Ueda M, Sorkina E, Valerio CM, Cochran E, Brown RJ, Peeden J, Tikhonovich Y, Tiulpakov A, Stender SRS, Klouda E, Tayeh MK, Innis J, Meyer A, Lal P, Godoy-Matos AF, Teles MG, Adams-Huet B, Rader DJ, Hegele RA, Oral EA, Garg A The Journal of clinical endocrinology and metabolism 2017 Dec -
Juvenile-onset generalized lipodystrophy due to a novel heterozygous missense LMNA mutation affecting lamin C.
Patni N, Xing C, Agarwal AK, Garg A American journal of medical genetics. Part A 2017 Jul -
The Diagnosis and Management of Lipodystrophy Syndromes: A Multi-Society Practice Guideline.
Brown RJ, Araujo-Vilar D, Cheung PT, Dunger D, Garg A, Jack M, Mungai L, Oral EA, Patni N, Rother K, von Schnurbein J, Sorkina E, Stanley T, Vigouroux C, Wabitsch M, Williams R, Yorifuji T The Journal of clinical endocrinology and metabolism 2016 Oct jc20162466 -
A 16-Year-Old Girl with Polyuria, Polydipsia, and a New-Onset Rash Around Her Elbows and Knees.
Patni N, Burton A Pediatric annals 2016 Sep 45 9 e317-8 -
Type 1 hyperlipoproteinemia in a child with large homozygous deletion encompassing GPIHBP1.
Patni N, Brothers J, Xing C, Garg A Journal of clinical lipidology 2016 Jul-Aug 10 4 1035-1039.e2 -
A Novel Syndrome of Generalized Lipodystrophy Associated With Pilocytic Astrocytoma.
Patni N, Alves C, von Schnurbein J, Wabitsch M, Tannin G, Rakheja D, Garg A The Journal of clinical endocrinology and metabolism 2015 Oct 100 10 3603-6 -
Congenital generalized lipodystrophies--new insights into metabolic dysfunction.
Patni N, Garg A Nature reviews. Endocrinology 2015 Sep 11 9 522-34 -
Worsening hypertriglyceridemia with oral contraceptive pills in an adolescent with HIV-associated lipodystrophy: a case report and review of the literature.
Patni N, Diaz EG, Cabral MD, Siqueira LM, Diaz A Journal of pediatric endocrinology & metabolism : JPEM 2014 Nov 27 11-12 1247-51 -
Elevated alpha-fetoprotein levels in Van Wyk-Grumbach syndrome: a case report and review of literature.
Patni N, Cervantes LF, Diaz A Journal of pediatric endocrinology & metabolism : JPEM 2012 25 7-8 761-7 -
YouTube as a source of information on the H1N1 influenza pandemic.
Pandey A, Patni N, Singh M, Sood A, Singh G American journal of preventive medicine 2010 Mar 38 3 e1-3 -
Association of exclusive smokeless tobacco consumption with hypertension in an adult male rural population of India.
Pandey A, Patni N, Sarangi S, Singh M, Sharma K, Vellimana AK, Patra S Tobacco induced diseases 2009 5 15 -
Assessment of risk and prophylaxis for deep vein thrombosis and pulmonary embolism in medically ill patients during their early days of hospital stay at a tertiary care center in a developing country.
Pandey A, Patni N, Singh M, Guleria R Vascular health and risk management 2009 5 643-8
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Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.
Research
- Type 1 Hyperlipoproteinemia
- Progeria syndromes
- Lipodystrophy syndromes
Results: 1 Locations
Children's Medical Center of Dallas
1935 Medical District DriveDallas, Texas 75235 214-730-5437 Directions to Children's Medical Center of Dallas