
Overview
Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan.
Dr. Priestley is highly rated in 21 conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Ornithine Transcarbamylase Deficiency, Biotinidase Deficiency, and Multiple Sulfatase Deficiency.
Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics. She is actively involved in clinical research, co-authoring 12 peer reviewed articles. Dr. Priestley is currently accepting new patients.
Specialties
Licenses
Board Certifications
Fellowships
Hospital Affiliations
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- HMO
- POS
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- EPO
- HMO
- POS
- PPO
Locations
25 Michigan Street Northeast, Suite 2100, Grand Rapids, MI 49503
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
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Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Adams is highly rated in 20 conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactose Epimerase Deficiency. Dr. Adams is currently accepting new patients.
Corewell Health Grand Rapids Hospitals Cancer Genetics - Lemmen-Holton
Paul Mark is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. Dr. Mark is highly rated in 4 conditions, according to our data. His clinical expertise encompasses VACTERL Association, Chromosome 21q Deletion, Peters Plus Syndrome, and Hypotonia. Dr. Mark is board certified in American Board Of Medical Genetics And Genomics. Dr. Mark is currently accepting new patients.
Frequently Asked Questions about Dr. Jessica R. Priestley
How do I make an appointment with Dr. Jessica R. Priestley?
You can book an appointment with Dr. Jessica R. Priestley by calling their office at 616-486-9830. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Jessica R. Priestley a top-rated expert for Fabry Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Jessica R. Priestley is classified as an Advanced expert for Fabry Disease, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Jessica R. Priestley specialize in?
While Dr. Jessica R. Priestley is a Pediatrics, they have specific expertise in Fabry Disease, Ornithine Transcarbamylase Deficiency, and Biotinidase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Pediatrics.
Does Dr. Jessica R. Priestley participate in research or clinical trials?
Yes. Dr. Jessica R. Priestley has published 12 articles and abstracts on conditions like Fabry Disease. You can view a list of Dr. Jessica R. Priestley's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Jessica R. Priestley accept my insurance?
Dr. Jessica R. Priestley accepts most major insurance plans, including Alignment Health Plan and Blue Cross Blue Shield. We recommend calling the office directly at 616-486-9830 to verify that your specific plan is currently accepted before your visit.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Autosomal Recessive Congenital Methemoglobinemia
- Biotinidase DeficiencyDr. Priestley isAdvanced. Learn about Biotinidase Deficiency.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Classic GalactosemiaDr. Priestley isAdvanced. Learn about Classic Galactosemia.
- Danon DiseaseDr. Priestley isAdvanced. Learn about Danon Disease.
- Dihydrolipoamide Dehydrogenase Deficiency
- Fabry DiseaseDr. Priestley isAdvanced. Learn about Fabry Disease.
- Galactose Epimerase DeficiencyDr. Priestley isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Priestley isAdvanced. Learn about Galactosemia.
- Kabuki SyndromeDr. Priestley isAdvanced. Learn about Kabuki Syndrome.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Multiple Sulfatase DeficiencyDr. Priestley isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Ornithine Transcarbamylase DeficiencyDr. Priestley isAdvanced. Learn about Ornithine Transcarbamylase Deficiency.
- Ornithine Translocase DeficiencyDr. Priestley isAdvanced. Learn about Ornithine Translocase Deficiency.
- PEPCK 1 DeficiencyDr. Priestley isAdvanced. Learn about PEPCK 1 Deficiency.
- Pompe DiseaseDr. Priestley isAdvanced. Learn about Pompe Disease.
- Pyruvate Carboxylase DeficiencyDr. Priestley isAdvanced. Learn about Pyruvate Carboxylase Deficiency.
- Pyruvate Decarboxylase DeficiencyDr. Priestley isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Priestley isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
- Experienced
- 15q11.2 MicrodeletionDr. Priestley isExperienced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Priestley isExperienced. Learn about 2q37 Deletion Syndrome.
- 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
- 3MC SyndromeDr. Priestley isExperienced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Priestley isExperienced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Priestley isExperienced. Learn about 47 XYY Syndrome.
- Aase SyndromeDr. Priestley isExperienced. Learn about Aase Syndrome.
- Abruzzo-Erickson SyndromeDr. Priestley isExperienced. Learn about Abruzzo-Erickson Syndrome.
- Acro-Pectoro-Renal Field DefectDr. Priestley isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- Acrodermatitis EnteropathicaDr. Priestley isExperienced. Learn about Acrodermatitis Enteropathica.
- Acropectoral SyndromeDr. Priestley isExperienced. Learn about Acropectoral Syndrome.
- Acrorenal Mandibular SyndromeDr. Priestley isExperienced. Learn about Acrorenal Mandibular Syndrome.
- Activated PI3K Delta Syndrome (APDS)Dr. Priestley isExperienced. Learn about Activated PI3K Delta Syndrome (APDS).
- Adams-Oliver SyndromeDr. Priestley isExperienced. Learn about Adams-Oliver Syndrome.
- Adrenoleukodystrophy (ALD)Dr. Priestley isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Allan-Herndon-Dudley SyndromeDr. Priestley isExperienced. Learn about Allan-Herndon-Dudley Syndrome.
- Alstrom SyndromeDr. Priestley isExperienced. Learn about Alstrom Syndrome.
- AminoaciduriaDr. Priestley isExperienced. Learn about Aminoaciduria.
- Arginase DeficiencyDr. Priestley isExperienced. Learn about Arginase Deficiency.
- Argininosuccinic AciduriaDr. Priestley isExperienced. Learn about Argininosuccinic Aciduria.
- Atelosteogenesis Type 1Dr. Priestley isExperienced. Learn about Atelosteogenesis Type 1.
- Athabaskan Brain Stem DysgenesisDr. Priestley isExperienced. Learn about Athabaskan Brain Stem Dysgenesis.
- Autism Spectrum DisorderDr. Priestley isExperienced. Learn about Autism Spectrum Disorder.
- Autosomal Cleft PalateDr. Priestley isExperienced. Learn about Autosomal Cleft Palate.
- Bardet-Biedl SyndromeDr. Priestley isExperienced. Learn about Bardet-Biedl Syndrome.
- Beare-Stevenson Cutis Gyrata SyndromeDr. Priestley isExperienced. Learn about Beare-Stevenson Cutis Gyrata Syndrome.
- Beckwith-Wiedemann SyndromeDr. Priestley isExperienced. Learn about Beckwith-Wiedemann Syndrome.
- Beta-Ketothiolase DeficiencyDr. Priestley isExperienced. Learn about Beta-Ketothiolase Deficiency.
- Birt-Hogg-Dube SyndromeDr. Priestley isExperienced. Learn about Birt-Hogg-Dube Syndrome.
- Blepharocheilodontic SyndromeDr. Priestley isExperienced. Learn about Blepharocheilodontic Syndrome.
- Bosma Arhinia Microphthalmia SyndromeDr. Priestley isExperienced. Learn about Bosma Arhinia Microphthalmia Syndrome.
- Bowen-Conradi SyndromeDr. Priestley isExperienced. Learn about Bowen-Conradi Syndrome.
- Brachydactyly Mononen TypeDr. Priestley isExperienced. Learn about Brachydactyly Mononen Type.
- Branchio-Oculo-Facial Syndrome (BOFS)Dr. Priestley isExperienced. Learn about Branchio-Oculo-Facial Syndrome (BOFS).
- Branchiootorenal SyndromeDr. Priestley isExperienced. Learn about Branchiootorenal Syndrome.
- C SyndromeDr. Priestley isExperienced. Learn about C Syndrome.
- Campomelia Cumming TypeDr. Priestley isExperienced. Learn about Campomelia Cumming Type.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Cantu SyndromeDr. Priestley isExperienced. Learn about Cantu Syndrome.
- Carbamoyl Phosphate Synthetase 1 DeficiencyDr. Priestley isExperienced. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- Cardiofaciocutaneous SyndromeDr. Priestley isExperienced. Learn about Cardiofaciocutaneous Syndrome.
- Cardiomyopathic LentiginosisDr. Priestley isExperienced. Learn about Cardiomyopathic Lentiginosis.
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Caudal Appendage DeafnessDr. Priestley isExperienced. Learn about Caudal Appendage Deafness.
- Caudal DuplicationDr. Priestley isExperienced. Learn about Caudal Duplication.
- Char SyndromeDr. Priestley isExperienced. Learn about Char Syndrome.
- CHARGE SyndromeDr. Priestley isExperienced. Learn about CHARGE Syndrome.
- ChondrodystrophyDr. Priestley isExperienced. Learn about Chondrodystrophy.
- Chromosome 11 Uniparental DisomyDr. Priestley isExperienced. Learn about Chromosome 11 Uniparental Disomy.
- Chromosome 12p DeletionDr. Priestley isExperienced. Learn about Chromosome 12p Deletion.
- Chromosome 13q DeletionDr. Priestley isExperienced. Learn about Chromosome 13q Deletion.
- Chromosome 15q DeletionDr. Priestley isExperienced. Learn about Chromosome 15q Deletion.
- Chromosome 18p DeletionDr. Priestley isExperienced. Learn about Chromosome 18p Deletion.
- Chromosome 2 Uniparental DisomyDr. Priestley isExperienced. Learn about Chromosome 2 Uniparental Disomy.
- Chromosome 21q DeletionDr. Priestley isExperienced. Learn about Chromosome 21q Deletion.
- Chromosome 4q DeletionDr. Priestley isExperienced. Learn about Chromosome 4q Deletion.
- Chromosome 6 Uniparental DisomyDr. Priestley isExperienced. Learn about Chromosome 6 Uniparental Disomy.
- Chromosome 6q DeletionDr. Priestley isExperienced. Learn about Chromosome 6q Deletion.
- Chromosome 6q DuplicationDr. Priestley isExperienced. Learn about Chromosome 6q Duplication.
- Chromosome 7p DeletionDr. Priestley isExperienced. Learn about Chromosome 7p Deletion.
- Chromosome 8p DeletionDr. Priestley isExperienced. Learn about Chromosome 8p Deletion.
- Chromosome 9p DeletionDr. Priestley isExperienced. Learn about Chromosome 9p Deletion.
- CitrullinemiaDr. Priestley isExperienced. Learn about Citrullinemia.
- Cockayne Syndrome Type 1Dr. Priestley isExperienced. Learn about Cockayne Syndrome Type 1.
- Cockayne Syndrome Type 2Dr. Priestley isExperienced. Learn about Cockayne Syndrome Type 2.
- Coffin-Lowry SyndromeDr. Priestley isExperienced. Learn about Coffin-Lowry Syndrome.
- Cohen SyndromeDr. Priestley isExperienced. Learn about Cohen Syndrome.
- ColobomaDr. Priestley isExperienced. Learn about Coloboma.
- Coloboma of IrisDr. Priestley isExperienced. Learn about Coloboma of Iris.
- Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limbs Defects
- Corpus Callosum AgenesisDr. Priestley isExperienced. Learn about Corpus Callosum Agenesis.
- Cortical DysplasiaDr. Priestley isExperienced. Learn about Cortical Dysplasia.
- Costello SyndromeDr. Priestley isExperienced. Learn about Costello Syndrome.
- Culler Jones SyndromeDr. Priestley isExperienced. Learn about Culler Jones Syndrome.
- Currarino TriadDr. Priestley isExperienced. Learn about Currarino Triad.
- De Barsy SyndromeDr. Priestley isExperienced. Learn about De Barsy Syndrome.
- Delayed GrowthDr. Priestley isExperienced. Learn about Delayed Growth.
- Dihydropteridine Reductase DeficiencyDr. Priestley isExperienced. Learn about Dihydropteridine Reductase Deficiency.
- Dilated Cardiomyopathy with Hypergonadotropic Hypogonadism
- Distal 18q Deletion SyndromeDr. Priestley isExperienced. Learn about Distal 18q Deletion Syndrome.
- DK Phocomelia SyndromeDr. Priestley isExperienced. Learn about DK Phocomelia Syndrome.
- DOOR SyndromeDr. Priestley isExperienced. Learn about DOOR Syndrome.
- Duane-Radial Ray SyndromeDr. Priestley isExperienced. Learn about Duane-Radial Ray Syndrome.
- Early Infantile Epileptic EncephalopathyDr. Priestley isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Familial Short Stature (FSS)Dr. Priestley isExperienced. Learn about Familial Short Stature (FSS).
- Fetal Akinesia SequenceDr. Priestley isExperienced. Learn about Fetal Akinesia Sequence.
- Filippi SyndromeDr. Priestley isExperienced. Learn about Filippi Syndrome.
- Floating-Harbor SyndromeDr. Priestley isExperienced. Learn about Floating-Harbor Syndrome.
- Focal or Multifocal Malformations in Neuronal Migration
- Frank Ter Haar SyndromeDr. Priestley isExperienced. Learn about Frank Ter Haar Syndrome.
- GABA-Transaminase DeficiencyDr. Priestley isExperienced. Learn about GABA-Transaminase Deficiency.
- Galactokinase DeficiencyDr. Priestley isExperienced. Learn about Galactokinase Deficiency.
- Gaucher DiseaseDr. Priestley isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Priestley isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Priestley isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Priestley isExperienced. Learn about Gaucher Disease Type 3.
- Glutaric Acidemia Type 1Dr. Priestley isExperienced. Learn about Glutaric Acidemia Type 1.
- Glycine EncephalopathyDr. Priestley isExperienced. Learn about Glycine Encephalopathy.
- Grix Blankenship Peterson SyndromeDr. Priestley isExperienced. Learn about Grix Blankenship Peterson Syndrome.
- Hardikar SyndromeDr. Priestley isExperienced. Learn about Hardikar Syndrome.
- Hemi 3 SyndromeDr. Priestley isExperienced. Learn about Hemi 3 Syndrome.
- HemihyperplasiaDr. Priestley isExperienced. Learn about Hemihyperplasia.
- Hennekam SyndromeDr. Priestley isExperienced. Learn about Hennekam Syndrome.
- HyperlysinemiaDr. Priestley isExperienced. Learn about Hyperlysinemia.
- Hypomelanosis of ItoDr. Priestley isExperienced. Learn about Hypomelanosis of Ito.
- HypospadiasDr. Priestley isExperienced. Learn about Hypospadias.
- Idiopathic Short Stature (ISS)Dr. Priestley isExperienced. Learn about Idiopathic Short Stature (ISS).
- Imperforate AnusDr. Priestley isExperienced. Learn about Imperforate Anus.
- Inborn Amino Acid Metabolism DisorderDr. Priestley isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Increased Head CircumferenceDr. Priestley isExperienced. Learn about Increased Head Circumference.
- Isovaleric AcidemiaDr. Priestley isExperienced. Learn about Isovaleric Acidemia.
- Jackson-Weiss SyndromeDr. Priestley isExperienced. Learn about Jackson-Weiss Syndrome.
- Jacobsen SyndromeDr. Priestley isExperienced. Learn about Jacobsen Syndrome.
- Johanson-Blizzard SyndromeDr. Priestley isExperienced. Learn about Johanson-Blizzard Syndrome.
- KBG SyndromeDr. Priestley isExperienced. Learn about KBG Syndrome.
- Keutel SyndromeDr. Priestley isExperienced. Learn about Keutel Syndrome.
- Klinefelter SyndromeDr. Priestley isExperienced. Learn about Klinefelter Syndrome.
- Koolen De Vries SyndromeDr. Priestley isExperienced. Learn about Koolen De Vries Syndrome.
- Lacrimo-Auriculo-Dento-Digital SyndromeDr. Priestley isExperienced. Learn about Lacrimo-Auriculo-Dento-Digital Syndrome.
- Leigh SyndromeDr. Priestley isExperienced. Learn about Leigh Syndrome.
- Lhermitte-Duclos DiseaseDr. Priestley isExperienced. Learn about Lhermitte-Duclos Disease.
- Lujan SyndromeDr. Priestley isExperienced. Learn about Lujan Syndrome.
- Malonyl-CoA Decarboxylase DeficiencyDr. Priestley isExperienced. Learn about Malonyl-CoA Decarboxylase Deficiency.
- Manitoba Oculotrichoanal SyndromeDr. Priestley isExperienced. Learn about Manitoba Oculotrichoanal Syndrome.
- Marshall SyndromeDr. Priestley isExperienced. Learn about Marshall Syndrome.
- Marshall-Smith SyndromeDr. Priestley isExperienced. Learn about Marshall-Smith Syndrome.
- Maternal HyperphenylalaninemiaDr. Priestley isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Mckusick-Kaufman SyndromeDr. Priestley isExperienced. Learn about Mckusick-Kaufman Syndrome.
- Megalencephaly-Capillary Malformation Syndrome
- MELAS SyndromeDr. Priestley isExperienced. Learn about MELAS Syndrome.
- MicrocephalyDr. Priestley isExperienced. Learn about Microcephaly.
- Microcephaly Deafness SyndromeDr. Priestley isExperienced. Learn about Microcephaly Deafness Syndrome.
- Mixed Gonadal DysgenesisDr. Priestley isExperienced. Learn about Mixed Gonadal Dysgenesis.
- Mosaic Variegated Aneuploidy SyndromeDr. Priestley isExperienced. Learn about Mosaic Variegated Aneuploidy Syndrome.
- Mucopolysaccharidoses (MPS)Dr. Priestley isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
- N-Acetylglutamate Synthase DeficiencyDr. Priestley isExperienced. Learn about N-Acetylglutamate Synthase Deficiency.
- Neu Laxova SyndromeDr. Priestley isExperienced. Learn about Neu Laxova Syndrome.
- Nevoid Basal Cell Carcinoma SyndromeDr. Priestley isExperienced. Learn about Nevoid Basal Cell Carcinoma Syndrome.
- Newborn JaundiceDr. Priestley isExperienced. Learn about Newborn Jaundice.
- Newborn Low Blood SugarDr. Priestley isExperienced. Learn about Newborn Low Blood Sugar.
- Nicolaides-Baraitser SyndromeDr. Priestley isExperienced. Learn about Nicolaides-Baraitser Syndrome.
- Nijmegen Breakage SyndromeDr. Priestley isExperienced. Learn about Nijmegen Breakage Syndrome.
- Noonan SyndromeDr. Priestley isExperienced. Learn about Noonan Syndrome.
- Oculodentodigital DysplasiaDr. Priestley isExperienced. Learn about Oculodentodigital Dysplasia.
- Oculodentodigital Dysplasia DominantDr. Priestley isExperienced. Learn about Oculodentodigital Dysplasia Dominant.
- Oculofaciocardiodental SyndromeDr. Priestley isExperienced. Learn about Oculofaciocardiodental Syndrome.
- Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant
- Pallister-Killian Mosaic SyndromeDr. Priestley isExperienced. Learn about Pallister-Killian Mosaic Syndrome.
- Periventricular HeterotopiaDr. Priestley isExperienced. Learn about Periventricular Heterotopia.
- Perlman SyndromeDr. Priestley isExperienced. Learn about Perlman Syndrome.
- Phenylketonuria (PKU)Dr. Priestley isExperienced. Learn about Phenylketonuria (PKU).
- PIK3CA-Related Overgrowth SpectrumDr. Priestley isExperienced. Learn about PIK3CA-Related Overgrowth Spectrum.
- Polysyndactyly Cardiac MalformationDr. Priestley isExperienced. Learn about Polysyndactyly Cardiac Malformation.
- Proteus SyndromeDr. Priestley isExperienced. Learn about Proteus Syndrome.
- Proteus-Like SyndromeDr. Priestley isExperienced. Learn about Proteus-Like Syndrome.
- RASopathiesDr. Priestley isExperienced. Learn about RASopathies.
- Retinopathy Pigmentary Mental RetardationDr. Priestley isExperienced. Learn about Retinopathy Pigmentary Mental Retardation.
- Rubinstein-Taybi SyndromeDr. Priestley isExperienced. Learn about Rubinstein-Taybi Syndrome.
- Ruvalcaba SyndromeDr. Priestley isExperienced. Learn about Ruvalcaba Syndrome.
- Scalp-Ear-Nipple SyndromeDr. Priestley isExperienced. Learn about Scalp-Ear-Nipple Syndrome.
- Schwartz-Jampel SyndromeDr. Priestley isExperienced. Learn about Schwartz-Jampel Syndrome.
- Short Stature (Growth Disorders)Dr. Priestley isExperienced. Learn about Short Stature (Growth Disorders).
- Simpson-Golabi-Behmel SyndromeDr. Priestley isExperienced. Learn about Simpson-Golabi-Behmel Syndrome.
- Smith-Kingsmore SyndromeDr. Priestley isExperienced. Learn about Smith-Kingsmore Syndrome.
- Snyder-Robinson SyndromeDr. Priestley isExperienced. Learn about Snyder-Robinson Syndrome.
- Spasmus NutansDr. Priestley isExperienced. Learn about Spasmus Nutans.
- Spontaneous Coronary Artery Dissection (SCAD)Dr. Priestley isExperienced. Learn about Spontaneous Coronary Artery Dissection (SCAD).
- Stickler SyndromeDr. Priestley isExperienced. Learn about Stickler Syndrome.
- Succinic Semialdehyde Dehydrogenase Deficiency
- Temple SyndromeDr. Priestley isExperienced. Learn about Temple Syndrome.
- Tetrasomy 9pDr. Priestley isExperienced. Learn about Tetrasomy 9p.
- Thymidine Kinase 2 Deficiency (TK2d)Dr. Priestley isExperienced. Learn about Thymidine Kinase 2 Deficiency (TK2d).
- Toriello-Carey SyndromeDr. Priestley isExperienced. Learn about Toriello-Carey Syndrome.
- Townes-Brocks SyndromeDr. Priestley isExperienced. Learn about Townes-Brocks Syndrome.
- Trichorhinophalangeal Syndrome Type 2Dr. Priestley isExperienced. Learn about Trichorhinophalangeal Syndrome Type 2.
- Turner SyndromeDr. Priestley isExperienced. Learn about Turner Syndrome.
- Urea Cycle Disorders (UCD)Dr. Priestley isExperienced. Learn about Urea Cycle Disorders (UCD).
- VACTERL AssociationDr. Priestley isExperienced. Learn about VACTERL Association.
- Van Maldergem SyndromeDr. Priestley isExperienced. Learn about Van Maldergem Syndrome.
- Vici SyndromeDr. Priestley isExperienced. Learn about Vici Syndrome.
- WAGR SyndromeDr. Priestley isExperienced. Learn about WAGR Syndrome.
- Weaver SyndromeDr. Priestley isExperienced. Learn about Weaver Syndrome.
- Wildervanck SyndromeDr. Priestley isExperienced. Learn about Wildervanck Syndrome.
- Woodhouse-Sakati SyndromeDr. Priestley isExperienced. Learn about Woodhouse-Sakati Syndrome.
- X-Linked Creatine DeficiencyDr. Priestley isExperienced. Learn about X-Linked Creatine Deficiency.
- X-Linked Spondyloepiphyseal Dysplasia TardaDr. Priestley isExperienced. Learn about X-Linked Spondyloepiphyseal Dysplasia Tarda.
- Y Chromosome InfertilityDr. Priestley isExperienced. Learn about Y Chromosome Infertility.
- Yunis-Varon SyndromeDr. Priestley isExperienced. Learn about Yunis-Varon Syndrome.

