Profile

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

Doctor Rating

4.9 out of 5

27 Ratings
1 Comments

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

  • B.S., University of the Sciences in Philadelphia , 1996
  • M.D., Penn State University College of Medicine , 2002
  • 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.

Memberships

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

NPI Number

  • 1013109594
Chad Haldeman-Englert, M.D.

Doctor Rating

4.9 out of 5

27 Ratings
1 Comments

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
Chad Haldeman-Englert, M.D.

Chad Haldeman-Englert, M.D.

Assistant Professor, Pediatrics

Doctor Rating

4.9 out of 5

Chad Haldeman-Englert, M.D.27 Ratings
1 Comments

Doctor Ratings

The overall Patient Rating score is the average of responses to the nine questions listed below. The questions are from the Press Ganey Patient Satisfaction Survey. Responses are measured on a 1 to 5 scale, where 1 represents "very poor" and 5 represents "very good."
Press Ganey Patient Satisfaction Survey

CP concern for questions/worries
4.9
CP efforts to include in decisions
5
CP explanations of prob/condition
4.9
CP spoke using clear language
5
Friendliness/courtesy of CP
5
Likelihood of recommending CP
4.9
Patients' confidence in CP
4.9
Time CP spent with patient
4.9
Wait time at clinic
4.4



Patient Comments

Comments are taken from the Care Provider section of the Press Ganey Patient Satisfaction Survey. Comments are posted exactly as they are written. Comments are added weekly. To protect patient privacy and confidentiality, patient names are not included.

5/7/2014

Good experience every time.

Quick Reference

Request an Appointment
New Patients

336-716-WAKE
888-716-WAKE

Existing patients may contact the clinic directly.
Find a Doctor Ways to Give
USNWR 2013-2014Magnet Hospital RecognitionConsumer Choice2014 Best DoctorsJoint Commission Report

Disclaimer: The information on this website is for general informational purposes only and SHOULD NOT be relied upon as a substitute for sound professional medical advice, evaluation or care from your physician or other qualified health care provider.