The 20 Best Klinefelter Syndrome Doctors Near Me in Baltimore, MD

Debra Counts is a Pediatric Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Counts is rated as a Distinguished provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 19 other conditions, according to our data. Her clinical expertise encompasses Idiopathic Short Stature (ISS), Klinefelter Syndrome, Short Stature (Growth Disorders), and Pediatric Growth Hormone Deficiency.

Dr. Dobs is presently an active clinical researcher in the field of endocrine gonadal function. She is particularly interested in new forms of male hormone replacement therapy and has published extensively in the area of hormonal changes with aging and chronic disease. Her clinical practice covers general endocrinology, with a focus on sex hormone disorders in both men and women. As Director of the Johns Hopkins Clinical Research Network, she oversees a multi-institutional consortium of hospitals in the mid-Atlantic states dedicated to facilitating clinical research through an academic-community hospital partnership. Dr. Dobs is rated as an Advanced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 9 other conditions, according to our data. Her clinical expertise encompasses Hypogonadism, Eunuchoidism Familial Hypogonadotropic, Testicular Failure, Isolated Hypogonadotropic Hypogonadism, and Hormone Replacement Therapy (HRT). Dr. Dobs is board certified in American Board Of Internal Medicine.

Dr. Herati is a urologist with fellowship training in male infertility and andrology. He has specialized training to perform complex reconstructions of the reproductive system, including vasectomy reversal with vasovasostomy and vasoepididymostomy. Additionally, he has an interest in treating patients with chronic prostatitis and pelvic pain, as well as patients experiencing low testosterone, erectile dysfunction, Peyronie’s disease and benign prostatic hyperplasia (BPH). Of note, he has the ability to perform fertility treatments on patients who have experienced spinal cord injuries using nonsurgical methods of sperm extraction. Dr. Herati believes in an individualized approach to care that addresses the whole patient. He invests significant time into building a rapport with his patients so that they feel comfortable opening up about these issues, allowing him to accurately identify and manage each patient’s needs. His research interests include decoding the genetic basis of male infertility, investigating the impact of referred pain from peripheral nerves to the bladder, and characterizing the effects of low testosterone on prostate inflammation and PSA screening. Dr. Herati sees patients at both the Johns Hopkins Hospital and The Johns Hopkins Bayview Medical Center. Videos Amin Herati, M.D.Urologist. Dr. Herati is rated as an Advanced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses Enlarged Prostate (BPH), Varicocele, Hypogonadism, Nephrectomy, and Prostatectomy. Dr. Herati is board certified in American Board Of Urology.

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 Klinefelter Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Epicanthal Folds, Strabismus, Hypotonia, and Brown Syndrome. Dr. Couser is board certified in American Board Of Medical Genetics And Genomics and American Board Of Ophthalmology.

Roopa Kanakatti Shankar, MD, MS, is a pediatric endocrinologist at Children’s National Hospital and an associate professor of pediatrics at the George Washington University School of Medicine and Health Sciences. Dr. Shankar specializes in working with children with Turner syndrome (TS). She leads the multidisciplinary Turner Syndrome Clinic, which is 1 of only 9 centers nationally and the only center in Washington, D.C., to be recognized by the Turner Syndrome Global Alliance (TSGA) for providing excellent care to individuals with TS and increasing knowledge about TS through research. Dr. Shankar holds board certifications in pediatrics and pediatric endocrinology, is the recipient of several honors, grants and awards, and is an active member of the Endocrine Society and the Pediatric Endocrine Society, including the Turner syndrome special interest group. Read more about Dr. Shankar’s research, including practice guidelines for Turner syndrome, at PubMed. Dr. Shankar is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses Turner Syndrome, Hypochondroplasia, Intersex, Mixed Gonadal Dysgenesis, and Hormone Replacement Therapy (HRT). Dr. Shankar is board certified in Pediatric Endocrinology: American Board Of Pediatrics, 2013 and Pediatrics: American Board Of Pediatrics, 2009.

David Fenig is a Urologist practicing medicine in Columbia, Maryland. Dr. Fenig is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 30 other conditions, according to our data. His clinical expertise encompasses Male Pseudohermaphroditism with Gynecomastia, Eunuchoidism Familial Hypogonadotropic, Testicular Failure, Hypogonadism Primary Partial Alopecia, and Ureteroscopy. Dr. Fenig is board certified in American Board Of Urology.

Dr. David W. Cooke is an associate professor of pediatrics at the Johns Hopkins University School of Medicine. Dr. Cooke’s clinical activities include both a general pediatric endocrine clinic and a pediatric diabetes clinic. His clinical interests include all endocrine disorders in children and adolescents, including short stature, abnormal pubertal development, growth hormone dysregulation, thyroid disorders, hormone deficiencies, hypopituitarism, diabetes insipidis, pituitary adenoma, prolactinoma, goiter, Cushing's disease, Addison's disease, polycystic ovary syndrome, congenital adrenal hyperplasia and disorders of sexual differentiation, Turner syndrome and Klinefelter syndrome, among others. He serves as clinical director of the division of pediatric endocrinology and director of the Pediatric Endocrinology Fellowship Training Program at Johns Hopkins. He is a member of the Johns Hopkins Klinefelter Syndrome Center. Dr. Cooke completed his undergraduate studies at the Massachusetts Institute of Technology, and received his medical degree from the Duke University School of Medicine. He then completed his residency in pediatrics at The Johns Hopkins Hospital, where he also completed a fellowship in pediatric endocrinology. He has been a faculty member in the Division of Pediatric Endocrinology at the Johns Hopkins since 1993. After his fellowship, Dr. Cooke spent five years of additional research training in the Department of Biological Chemistry at Johns Hopkins, supported by an individual Physician Scientist Award from the National Institutes of Health (NIH). Dr. Cooke’s past research interest was the molecular basis of insulin resistance and obesity, with studies examining the role the adipocyte plays in these conditions. He had received research funding for these studies from the NIH and from the American Diabetes Association. Dr. Cooke is a recipient of the Johns Hopkins University School of Medicine Institute for Excellence in Education award for Outstanding Achievement in Medical and Biomedical Education. He also has been recognized as a Top Doctor by Baltimore magazine. Dr. Cooke is a member of the Society for Pediatric Research, the American Diabetes Association, the Endocrine Society and Pediatric Endocrinology Society. He is a fellow of the American Academy of Pediatrics. Dr. Cooke is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. His clinical expertise encompasses Klinefelter Syndrome, Type 1 Diabetes (T1D), Precocious Puberty, and Diabetic Ketoacidosis. Dr. Cooke is board certified in American Board Of Pediatrics.

Melissa Pagan is a Pediatrics provider practicing medicine in Baltimore, Maryland. Dr. Pagan is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Short Stature (Growth Disorders), Familial Short Stature (FSS), Idiopathic Short Stature (ISS), and Precocious Puberty.

Kayur Bhavsar is an Endocrinologist practicing medicine in Frederick, Maryland. Dr. Bhavsar is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Thyroid Nodule, Hypothyroidism, and Hypercalcemia.

Ryan Miller is a Pediatric Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Miller is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Short Stature (Growth Disorders), Idiopathic Short Stature (ISS), Familial Short Stature (FSS), and Pediatric Growth Hormone Deficiency.

Mansur Shomali is an Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Shomali is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 4 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Paget's Disease of Bone, and Type 1 Diabetes (T1D).

Salman Bhat is an Endocrinologist practicing medicine in Salisbury, Maryland. Dr. Bhat is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 11 other conditions, according to our data. His clinical expertise encompasses Type B Insulin Resistance Syndrome, Type 2 Diabetes (T2D), Low Blood Sugar, and Thyroid Storm.

Dominique Long is a Pediatric Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Long is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Short Stature (Growth Disorders), Familial Short Stature (FSS), Idiopathic Short Stature (ISS), and Growth Hormone Deficiency (GHD).

Paula Newton is a Pediatric Endocrinologist practicing medicine in Baltimore, Maryland. Dr. Newton is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 10 other conditions, according to our data. Her clinical expertise encompasses Short Stature (Growth Disorders), Familial Short Stature (FSS), Idiopathic Short Stature (ISS), and Precocious Puberty.

Tadele Desalew is an Endocrinologist practicing medicine in Waldorf, Maryland. Dr. Desalew is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 16 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Hypothyroidism, Thyroid Storm, and Hyperthyroidism.

Maximilian Muenke is a Medical Genetics provider practicing medicine in Bethesda, Maryland. Dr. Muenke is rated as an Advanced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 13 other conditions, according to our data. His clinical expertise encompasses Holoprosencephaly, Turner Syndrome, Corpus Callosum Agenesis, and Chromosome 7q Duplication.

Kenneth Rosenbaum, MD, started with Children’s National Hospital in 1972 after completing his medical genetics training at Johns Hopkins University in 1971. Dr. Rosenbaum has consistently been voted the top physician at Children’s National over the past 10 years. Dr. Rosenbaum has overseen dysmorphic research projects at the National Institutes of Health, in Egypt, and here at Children’s National. Dr. Rosenbaum is the co-director of the Down Syndrome Clinic and the NF clinic. Dr. Rosenbaum is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 3 other conditions, according to our data. His clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Neurofibromatosis, Triple X Syndrome, and Williams Syndrome. Dr. Rosenbaum is board certified in Clinical Cytogenetics: American Board Of Medical Genetics And Genomics, 1982, Clinical Genetics (MD): American Board Of Medical Genetics And Genomics, 1982, and Pediatrics: American Board Of Pediatrics, 1976.

Vikram Shenoy, M.D., practices endocrinology at Johns Hopkins Community Physicians Downtown Bethesda. He received his medical degree from University of Connecticut School of Medicine, and also completed his residency in endocrinology at Hospital of the University of Pennsylvania. He practices general endocrinology, including the treatment of thyroid disorders, diabetes, PCOS, pituitary and adrenal disorders, hypogonadism and osteoporosis. Dr. Shenoy is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. He is also highly rated in 19 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Type 1 Diabetes (T1D), and Hypothyroidism. Dr. Shenoy is board certified in American Board Of Internal Medicine.

Dr. Malinda Wu is a pediatric endocrinologist seeing patients at the Johns Hopkins Children’s Center in Baltimore, Maryland. She specializes in a wide range of pediatric endocrine conditions including metabolic bone disease, pediatric osteoporosis and cystic fibrosis endocrinopathies. Dr. Wu received her M.D. from Jefferson Medical College, Thomas Jefferson University. She completed pediatrics residency at Penn State Hershey Medical Center and her pediatric endocrine fellowship at Emory University School of Medicine. She received her Master of Science in Clinical Research from Emory University (2021). Dr. Wu has been a faculty member at Johns Hopkins since 2021. Dr. Wu’s research interests are in metabolic bone disease and the health of women with cystic fibrosis. Dr. Wu’s current research is focused on women with cystic fibrosis and how estrogen supplementation may impact their health. She has received grant funding from the Cystic Fibrosis Foundation. Dr. Wu is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Osteogenesis Imperfecta, Hypogonadism, Familial Glucocorticoid Deficiency, Exocrine Pancreatic Insufficiency, and Hormone Replacement Therapy (HRT). Dr. Wu is board certified in American Board Of Pediatrics.

Pim Suwannarat is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Frederick, Maryland. Dr. Suwannarat is rated as an Experienced provider by MediFind in the treatment of Klinefelter Syndrome. She is also highly rated in 2 other conditions, according to our data. Her clinical expertise encompasses Triple X Syndrome, Classic Galactosemia, Ehlers-Danlos Syndrome (EDS), and Chromosome 10q Deletion. Dr. Suwannarat is currently accepting new patients.