AngelikaLudtke(Ludtke)ErwinMDPhD

Clinical Genetics

Interim Medical Director, Center for Personalized Genetic Healthcare, Cleveland Clinic; Founder and director, MyGeneticist, Miami

Dr. Erwin is on Doximity

As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.

Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
Connect with colleagues in the same hospital or clinic.
Read the latest clinical news, personalized to your specialty.

Office
8500 SW 92nd St
MyGeneticist, Suite 101
Miami, FL 33156
Phone+1 786-388-0600

Fax+1 305-667-1675

Dr. Angelika Erwin is a medical geneticist in Miami, FL and is affiliated with Cleveland Clinic. She received her medical degree from Charité- Universitätsmedizin Berlin and has been in practice 14 years. She also speaks multiple languages, including German, Spanish, and French. She specializes in clinical genetics and is experienced in lysosomal storage diseases, cancer genetics, general medical genetics, lipodystrophy, and porphyrias.

Icahn School of Medicine at Mount SinaiResidency, Internal Medicine/Medical Genetics and Genomics, 2008 - 2013
Icahn School of Medicine at Mount Sinai/Mount Sinai HospitalResidency, Internal Medicine, 2011
Charité - Universitätsmedizin BerlinClass of 2003

PubMed

Contemporary Multimodality Imaging for Diagnosis and Management of Fabry Cardiomyopathy.
Simrat Kaur, Jaideep Singh Bhalla, Angelika L Erwin, Wael Jaber, Tom Kai Ming Wang
Journal of Clinical Medicine. 2024-08-14
Congenital erythropoietic porphyria.
Jordi To-Figueras, Angelika L Erwin, Paula Aguilera, Oscar Millet, Robert J Desnick
Liver International. 2024-08-01
4 citations
Evidence-based consensus guidelines for the diagnosis and management of protoporphyria-related liver dysfunction in erythropoietic protoporphyria and X-linked protopor...
Cynthia Levy, Amy K Dickey, Bruce Wang, Manish Thapar, Hetanshi Naik
Hepatology. 2024-03-01

Journal Articles

De Novo Missense Variants in MEIS2 Recapitulate the Microdeletion Phenotype of Cardiac and Palate Abnormalities, Developmental Delay, Intellectual Disability and Dysmo...
Theresa Grebe, Susan Winter, Elaine H Zackai, Angelika L Erwin, Matthew A Deardorff, Margaret Harr, American Journal of Medical Genetics Part A
Congenital Erythropoietic Porphyria.
Erwin A., Balwani M., Desnick R.J., GeneReviews™, 2013
Thiazolidinedione Response in Familial Lipodystrophy Patients with LMNA Mutations: A Case Series.
Luedtke A, Boschmann M, Colpe C, Engeli S, Adams F, Birkenfeld AL, Haufe S, Rahn G, Luft FC, Schmidt HH, Jordan J., Hormone and Metabolic Research, 2012

New Drug May Treat Rare Diseases That Make Exposure to Sunlight PainfulApril 13th, 2023
Alnylam to Present Full 9-Month Results from the HELIOS-A Phase 3 Study of Vutrisiran at the American Academy of Neurology Virtual Annual Meeting 2021March 23rd, 2021
Treatment and Medication Options for Fabry DiseaseAugust 23rd, 2023