Chad Haldeman-Englert, M.D., Assistant Professor Pediatrics

Chad Haldeman-Englert, M.D.

Assistant Professor, Pediatrics

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

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

Assistant Professor, Pediatrics

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

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.