Profile

Chad Haldeman-Englert, M.D.Wake Forest Baptist Health

Chad Haldeman-Englert, M.D.

Assistant Professor,

Clinical Specialties

Cleft Lip and Palate, Inborn Errors of Metabolism, Genetics, Dysmorphology, Craniofacial Malformation, Chromosome 22q11 Deletion Syndrome

Contact Information

New Patient Appointments: 336-716-WAKE
Returning Patient Appointments: 336-713-4500
Department: 336-713-4500

Email: chaldema@wakehealth.edu

Insurance Accepted »

Education & Training

  • M.D., Penn State University College of Medicine , 2002
  • B.S., University of the Sciences in Philadelphia , 1996
  • Fellowship, Medical Genetics, Children's Hospital of Philade, 2009

Board Certifications

  • American Board of Internal Medicine, Internal Medicine - Internal Medicine
  • American Board of Medical Genetics, Medical Genetics - Clinical Genetics - M.D.
  • American Board of Pediatrics, Pediatrics, Pediatrics - Pediatrics

Memberships

  • North Carolina Medical Genetic
  • Am Soc Of Human Genetics
  • Alpha Omega Alpha

NPI Number

  • 1013109594
Chad Haldeman-Englert, M.D.Wake Forest Baptist Health

Chad Haldeman-Englert, M.D.

Assistant Professor, Pediatrics

Contact Information

Academic: 336-713-7525 | Department: 336-713-4500

Email: chaldema@wakehealth.edu

Recent Publications

Tuz K, Bachmann-Gagescu R, O'Day DR, Hua K, Isabella CR, Phelps IG, Stolarski AE, O'Roak BJ, Dempsey JC, Lourenco C, Alswaid A, Bonnemann CG, Medne L, Nampoothiri S, Stark Z, Leventer RJ, Topcu M, Cansu A, Jagadeesh S, Done S,. Mutations in CSPP1 cause primary cilia abnormalities and Joubert syndrome with or without Jeune asphyxiating thoracic dystrophy. Am J Hum Genet. 2014;94(1):62-72.

Delio M, Pope K, Wang T, Samanich J, Haldeman-Englert CR, Kaplan P, Shaikh TH, Cai J, Marion RW, Morrow BE, Babcock M. Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome. Am J Med Genet A. 2013;161A(3):527-533.

Mark PR, Radlinski BC, Core N, Fryer A, Kirk EP, Haldeman-Englert CR. Narrowing the critical region for congenital vertical talus in patients with interstitial 18q deletions. Am J Med Genet A. 2013;161A(5):1117-1121.

Haldeman-Englert CR, Biser A, Zackai EH, Ming JE. Revision of 'A 223-kb de novo deletion of PAX9 in a patient with oligodontia'. J Craniofac Surg. 2012;23(2):e149-151.

Kuppler KM, Kirse DJ, Thompson JT, Haldeman-Englert CR. Loeys-Dietz syndrome presenting as respiratory distress due to pulmonary artery dilation. Am J Med Genet A. 2012;158A(5):1212-1215.

Izumi K, Conlin LK, Berrodin D, Fincher C, Wilkens A, Haldeman-Englert C, Saitta SC, Zackai EH, Spinner NB, Krantz ID. Duplication 12p and Pallister-Killian syndrome: a case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region. Am J Med Genet A. 2012;158A(12):3033-3045.

Shaikh TH, Haldeman-Englert C, Geiger EA, Ponting CP, Webber C. Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes. Hum Mol Genet. 2011;20(5):880-893.

Boyadjiev SA, Kim S-D, Hata A, Haldeman-Englert C, Zackai EH, Naydenov C, Hamamoto S, Schekman RW, Kim J. Cranio-lenticulo-sutural dysplasia associated with defects in collagen secretion. Clin Genet. 2011;80(2):169-176.

Haldeman-Englert CR, Biser A, Zackai EH, Ming JE. A 223-kb de novo deletion of PAX9 in a patient with oligodontia. J Craniofac Surg. 2010;21(3):837-839.

Sheridan MB, Kato T, Haldeman-Englert C, Jalali GR, Milunsky JM, Zou Y, Klaes R, Gimelli G, Gimelli S, Gemmill RM, et al. A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21). Am J Hum Genet. 2010;87(2):209-218.

All Publications

For a listing of recent publications, refer to PubMed, a service provided by the National Library of Medicine.

For a list of earlier publications, visit the Carpenter Library Publication Search.

Assistant Professor, Pediatrics

Clinical Specialties

Cleft Lip and Palate, Inborn Errors of Metabolism, Genetics, Dysmorphology, Craniofacial Malformation, Chromosome 22q11 Deletion Syndrome

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