The 20 Best Mucolipidosis 3 Doctors in The United States

Cynthia Tifft is a Medical Genetics provider in Washington, Washington, D.c.. Dr. Tifft is rated as an Elite provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Sandhoff Disease, Gangliosidosis, GM1 Gangliosidosis, and Tay-Sachs Disease.

Sara Cathey is a Medical Genetics provider in Charleston, South Carolina. Dr. Cathey is rated as a Distinguished provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Aspartylglucosaminuria, Mucolipidosis Type 4, Fucosidosis, and Sialidosis. Dr. Cathey is currently accepting new patients.

. Dr. Perszyk is rated as an Advanced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Mucolipidosis 3.

Raymond Wang is a Medical Genetics provider in Orange, California. Dr. Wang is rated as an Advanced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Mucopolysaccharidoses (MPS), Mucopolysaccharidosis Type 7 (MPS VII, Sly Syndrome), Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome), Pompe Disease, and Adenoidectomy.

Jaime Barea is a Medical Genetics provider in Madera, California. Dr. Barea is rated as a Distinguished provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Mucolipidosis Type 4, Sialidosis, Mucolipidosis 3, and Propionic Acidemia.

Lynne Bird is a Medical Genetics specialist and a Pediatrics provider in San Diego, California. Dr. Bird is rated as a Distinguished provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Angelman Syndrome, Prader-Willi Syndrome, VACTERL Association, and Mucolipidosis Type 4.

Angelika Erwin is a Pediatrics provider in Cleveland, Ohio. Dr. Erwin is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, Gaucher Disease Type 3, and Gaucher Disease Type 1.

Dr. Couser obtained his bachelor’s degree from the University of Virginia and his Medical Doctorate from the Virginia Commonwealth University School of Medicine (VCU SOM). Dr. Couser’s ophthalmology residency was completed at Howard University where he served as co-chief resident in the last year of his residency. He received fellowship training in pediatric ophthalmology and adult strabismus at Emory University. Dr. Couser received a master’s degree in biotechnology from the Johns Hopkins University and completed a residency in clinical genetics at the University of North Carolina at Chapel Hill. He is one of only a few individuals currently board-certified by both the American Board of Ophthalmology and the American Board of Medical Genetics and Genomics. CV https://www.hopkinsmedicine.org/-/media/wilmer/documents/cvs/couser-cv Research Summary My primary research focus involves the identification and management of genetic eye diseases including rare inherited disorders affecting the eyes. Research and scholarly activities have been an integral component of my career path. I have been the principal investigator on 10 clinical trial/IRB studies and a co-investigator on others, participated with several committees or advisory panels related to research activities. I have been credited with over 120 book chapter, journal article and abstract publications. In addition, I served as the primary author/sole editor for a textbook titled Ophthalmic Genetic Diseases: A Quick Reference Guide to the Eye and External Ocular Adnexa Abnormalities, 1st Edition, published by Elsevier in 2018, which is one of only a few textbooks published in this subject area. I also served as a grant review panelist for the National Eye Institute Career Development Awards. Selected Publications *Couser NL, Masood MM, Strande NT, Foreman AKM, Crooks K, Weck KE, Lu M, Wilhelmsen KC, Roche M, Evans JP, Berg JS, Powell CM. 2015. The phenotype of multiple congenital anomalies- hypotonia-seizures syndrome 1: Report and review. Am J Med Genet Part A 9999A:1–6 *Couser NL, Lambert SR. Botulinum toxin: A treatment of consecutive esotropia in children. Strabismus 2012; 20(4):158-161 Couser NL, Lenhart PD, Hutchinson AK. Augmented Hummelsheim procedure to treat complete abducens nerve palsy. J AAPOS 2012;16(4):331-5 *Natario L. Couser, Maheer M. Masood, Arthur S. Aylsworth, and Roger E. Stevenson. Ocular manifestations in the X-linked intellectual disability syndromes. Ophthalmic Genet. 2017, Jan 23:1-12 *Couser NL, Brooks BP, Drack AV, Shankar SP. The evolving role of genetics in ophthalmology. Ophthalmic Genet. 2021 Jan 12:1-4. doi: 10.1080/13816810.2020.1868011. Dr. Couser is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Epicanthal Folds, Strabismus, Hypotonia, and Brown Syndrome.

Dr. Ian Daniel Krantz, MD, is a renowned physician specializing in Genetics and Pediatrics. He currently sees patients at Cohen Children's Medical Center (CCMC) and Northwell Health Physician Partners Medical Genetics. Dr. Krantz holds certifications in Clinical Genetics, Cytogenetics, and Pediatrics from the American Board of Medical Genetics and the American Board of Pediatrics, respectively.Dr. Krantz completed his BFA at Concordia University in Montreal and his MD at Sackler School of Medicine (Tel Aviv University). He completed his residency in Medical Genetics at Children's Hospital of Philadelphia and his residency in Pediatrics at New York University Medical Center.With an impressive set of academic and administrative titles, Dr. Krantz serves as the Division Chief of Pediatric Genetics and Genomics at Cohen Children's Medical Center and is the System Vice President for Pediatric Genetics at Northwell Health. Additionally, he holds the position of Professor at the Zucker School of Medicine at Northwell Health.Dr. Krantz is recognized for his clinical expertise in isolated and syndromic forms of congenital birth differences and developmental diagnoses, including syndromic and non-syndromic autism. He has a special interest in the genetics of hearing loss and focused expertise in Cornelia de Lange Syndrome, Pallister-Killian syndrome, Alagille syndrome, CHOPS syndrome, among others.Dr. Krantz's research is dedicated to identifying and characterizing the molecular etiology of syndromic and non-syndromic developmental diagnoses. His research lab has made significant contributions in the field, discovering new disease genes and shedding light on critical molecular pathways involved in human developmental disorders.Driven by his commitment to advancing patient care, Dr. Krantz has been at the forefront of integrating genomic technologies into the clinical setting. He has implemented rapid genome sequencing into the NICU and CICU and established biobanks and biorepositories to further research efforts. Through his work, he aims to understand the impact of complex diagnostic information on clinicians and families involved.With his extensive expertise and dedication to advancing genetic research and patient care, Dr. Krantz continues to make significant contributions to the field of Pediatrics and Genetics. Dr. Krantz is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Cornelia De Lange Syndrome, Pallister-Killian Mosaic Syndrome, Mosaicism, and KBG Syndrome.

Laura Mackay is a Medical Genetics provider in Dallas, Texas. Dr. Mackay is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Isovaleric Acidemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD).

Carlos Mares-Beltran is a Medical Genetics specialist and a Pediatrics provider in Albany, New York. Dr. Mares-Beltran is rated as an Advanced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Mucolipidosis 3, Maternal Hyperphenylalaninemia, Dihydropteridine Reductase Deficiency, and Tetrasomy 9p.

Barbara Burton is a Medical Genetics specialist and a Pediatrics provider in Chicago, Illinois. Dr. Burton is rated as an Advanced provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Phenylketonuria (PKU), Mucopolysaccharidoses (MPS), and Cholesteryl Ester Storage Disease.

Timothy Wood is a Medical Genetics provider in Greenwood, South Carolina. Dr. Wood is rated as an Advanced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Mucolipidosis Type 4, Sialidosis, Mucolipidosis 3, and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).

Michael Friez is a Medical Genetics provider in Greenwood, South Carolina. Dr. Friez is rated as an Advanced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Rett Syndrome, Mucolipidosis Type 4, Autism Spectrum Disorder, and Scalp-Ear-Nipple Syndrome.

Benjamin Ellezam practices in Houston, Texas. Dr. Ellezam is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Myositis, Necrotizing Myopathy (NM), Gliomatosis Cerebri, and Glioma.

Molly Mcpheron is a Medical Genetics specialist and a Pediatrics provider in Indianapolis, Indiana. Dr. Mcpheron is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Ornithine Transcarbamylase Deficiency, Pompe Disease, Phenylketonuria (PKU), and Danon Disease. Dr. Mcpheron is currently accepting new patients.

Walla Al-Hertani is a Medical Genetics provider in Orange, California. Dr. Al-Hertani is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Von Gierke Disease, Classic Galactosemia, Phosphoglycerate Mutase Deficiency, and Glycogen Storage Disease Type 7. Dr. Al-Hertani is currently accepting new patients.

Raymond Lewandowski is a Medical Genetics provider in Richmond, Virginia. Dr. Lewandowski is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Brittle Cornea Syndrome, Vascular Ehlers-Danlos Syndrome (VEDS), Increased Head Circumference, and Danon Disease. Dr. Lewandowski is currently accepting new patients.

Robert Hopkin is a Medical Genetics specialist and a Pediatrics provider in Cincinnati, Ohio. Dr. Hopkin is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. His top areas of expertise are Fabry Disease, Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Microcephaly, and Orchiectomy.

Kristina Cusmano-Ozog is a Medical Genetics specialist and a Pediatrics provider in Stanford, California. Dr. Cusmano-Ozog is rated as an Experienced provider by MediFind in the treatment of Mucolipidosis 3. Her top areas of expertise are Maple Syrup Urine Disease, Mucolipidosis Type 4, Grix Blankenship Peterson Syndrome, and Micrognathia.