The 20 Best Chromosome 4q Deletion Doctors Near Me

. Dr. Russi is rated as an Advanced provider by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Increased Head Circumference, Ehlers-Danlos Syndrome (EDS), Chromosome 8p Deletion, and Chromosome 6q Duplication.

. Dr. Narumanchi is rated as an Advanced provider by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, and Maternal Hyperphenylalaninemia.

Erica Fernandes is a Medical Genetics specialist and a Pediatrics provider in New Hyde Park, New York. Dr. Fernandes is rated as an Advanced provider by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Microcephaly, Chromosome 13q Deletion, Bowen-Conradi Syndrome, and Floating-Harbor Syndrome.

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

. Dr. Melnyk is rated as an Experienced provider by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Ehlers-Danlos Syndrome (EDS), Musculocontractural Ehlers-Danlos Syndrome (mcEDS), Jacobsen Syndrome, and Chromosome 6q Deletion.

Fang Fu practices in Luoyang, China. Fu is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. Their top areas of expertise are Chromosome 4q Deletion, Ventricular Septal Defects, Fetal Edema, and Hydrops Fetalis.

Laura Mary practices in Rennes, France. Ms. Mary is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Chromosome 4q Deletion, Bardet-Biedl Syndrome, Chromosome 6q Duplication, and Focal Dermal Hypoplasia.

Zivile Maldziene practices in Vilnius, Lithuania. Maldziene is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. Their top areas of expertise are Chromosome 4q Deletion, Greig Cephalopolysyndactyly Syndrome, Iridogoniodysgenesis Type 1, and Feingold Syndrome.

Panlai Shi practices in Zhengzhou, China. Shi is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. Their top areas of expertise are Chromosome 4q Deletion, Mosaicism, Chromosome 15q Duplication, and Polyhydramnios.

Gil Filho-Novo practices in Sao Paulo, Brazil. Mr. Filho-Novo is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Chromosome 4q Deletion, Bloom Syndrome, Trisomy 12 Mosaicism, and Collagen VI-Related Myopathy.

Fei Liang practices in Xi'an, China. Liang is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. Their top areas of expertise are Chromosome 4q Deletion, Thymic Epithelial Tumor, Cholangiocarcinoma (Bile Duct Cancer), Thymectomy, and Lithotripsy.

Zsolt Tidrenczel practices in Magyar Honvédség Egészségügyi Központ Budapest, Puerto Rico. Mr. Tidrenczel is rated as a Distinguished expert by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Chromosome 4q Deletion, Pallister-Killian Mosaic Syndrome, Trisomy 12 Mosaicism, and Micrognathia.

Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider in Dallas, Texas. Dr. Scheuerle is rated as an Advanced provider by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.

Luis Umana is a Medical Genetics specialist and a Pediatrics provider in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Classic Galactosemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Biotinidase Deficiency, and Argininosuccinic Aciduria.

Carolyn Jones is a Medical Genetics provider in Winfield, Illinois. Dr. Jones has been practicing medicine for over 35 years and is rated as an Advanced provider by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Fabry Disease, Megalencephalic Leukoencephalopathy with Subcortical Cysts, Multiple Sulfatase Deficiency, and Pompe Disease.

Linda Rossetti is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Rossetti has been practicing medicine for over 10 years and is rated as an Experienced provider by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Smith-Magenis Syndrome, Miller-Dieker Syndrome, Chromosome 6q Duplication, and Chromosome 8p Deletion.

Peter Hulick, MD, a clinical geneticist and chair of personalized medicine at Endeavor Health, helps patients understand how genomic information can inform care and improve health outcomes. With a career rooted in genetics since high school, he works to integrate genomic data into everyday decision-making for patients and clinicians. Dr. Hulick focuses on risk assessment, early detection and treatment guidance by combining science, patient context and team collaboration. He also leads efforts to make genomic care more accessible across the health system. Dr. Hulick is rated as an Experienced provider by MediFind in the treatment of Chromosome 4q Deletion. His top areas of expertise are Ehlers-Danlos Syndrome (EDS), Ring Chromosome 12, Retinopathy Pigmentary Mental Retardation, and BRCA Positive Breast Cancer.

Theresa Grebe is a Pediatrics provider in Phoenix, Arizona. Dr. Grebe is rated as an Experienced provider by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Chromosome 6 Uniparental Disomy, Temple Syndrome, Hypotonia, and Congenital Bowing of Long Bones. Dr. Grebe is currently accepting new patients.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider in Grand Rapids, Michigan. Dr. Priestley has been practicing medicine for over 8 years and is rated as an Experienced provider by MediFind in the treatment of Chromosome 4q Deletion. Her top areas of expertise are Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Megalencephalic Leukoencephalopathy with Subcortical Cysts.

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 Chromosome 4q Deletion. His top areas of expertise are Epicanthal Folds, Strabismus, Brown Syndrome, and Hypotonia.