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Dr. Neena Champaigne, MD

Charleston, SC

Accepting patients

Affiliated with a Castle Connolly Top Hospital

    Who is Dr. Champaigne, Clinical Geneticist in Charleston, SC?

    Dr. Neena Champaigne, MD is a Clinical Geneticist, who primarily practices in Charleston, SC with 2 additional practice locations. She is board certified by the American Board of Medical Genetics and American Board of Pediatrics. Dr. Champaigne graduated from Texas A&M University. Dr. Champaigne is fluent in English and Spanish, and is currently seeing new patients. Dr. Champaigne’s practice accepts Cigna, Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Champaigne’s office at (843) 792-1414.

    Where did Dr. Champaigne go to medical school and complete their residency?

    • Medical School: Texas A&M University

    Is Dr. Champaigne board certified in Clinical Geneticist?

    Yes, Dr. Neena Champaigne, MD is board certified by the American Board of Medical Genetics , American Board of Pediatrics

    What languages does Dr. Champaigne speak?

    Dr. Champaigne and their clinical team can communicate with patients in the following languages:

    • English

    • Spanish

    What conditions does Dr. Champaigne treat?

    As a Clinical Geneticist, Dr. Champaigne diagnoses, treats, and manages a wide range of conditions. This condition information is derived from anonymized insurance claims and highlights the medical conditions most commonly treated by Dr. Champaigne. It provides insight into the doctor’s areas of experience and expertise based on real-world patient encounters from the past two years, updated quarterly.

    Also known as:

    • Pompe Disease
    • Glycogen Storage Disease Type I
    • Carbohydrate Metabolism Disorder
    • Pompe disease
    • Glycogen storage disease type I
    • GSD II
    • Glycogen Storage Disease Type II
    • Acid Maltase Deficiency
    • von Gierke Disease
    • GSD I
    • Hepatorenal Glycogenosis

    ICD-10 Codes:

    • E7402: Pompe disease
    • E7401: von Gierke disease

    Also known as:

    • Birth Defects Causing Overgrowth
    • Other Genetic Syndrome
    • Other Birth Defects Causing Short Stature
    • Birth Defects
    • Overgrowth Syndromes
    • Congenital Gigantism
    • Rare Birth Defect Syndromes
    • Uncommon Congenital Syndromes
    • Rare Short Stature Syndromes
    • Uncommon Dwarfism

    ICD-10 Codes:

    • Q873: Congenital malformation syndromes involving early overgrowth
    • Q8789: Other specified congenital malformation syndromes, not elsewhere classified
    • Q8719: Other congenital malformation syndromes predominantly associated with short stature

    Also known as:

    • Autism
    • Autism Spectrum Disorder
    • Classic Autism', 'Kanner's Syndrome
    • Severe Autism

    ICD-10 Codes:

    • F840: Autistic disorder

    Also known as:

    • Argininosuccinic Aciduria
    • High Phenylalanine Levels
    • Metabolic Disorder
    • Argininosuccinic aciduria
    • Tetrahydrobiopterin deficiency
    • Argininosuccinic Acid Lyase Deficiency
    • ASA Lyase Deficiency
    • Hyperphenylalaninemia
    • Phenylalanine Metabolism Disorder
    • Phenylketonuria (PKU)

    ICD-10 Codes:

    • E7222: Arginosuccinic aciduria
    • E701: Other hyperphenylalaninemias

    Also known as:

    • Other Developmental Disabilities
    • Unspecified Developmental Disability
    • Developmental Disabilities
    • Atypical psychological development
    • Unspecified developmental disorder
    • Global developmental delay
    • Psychological development disorder

    ICD-10 Codes:

    • F88: Other disorders of psychological development
    • F89: Unspecified disorder of psychological development

    Also known as:

    • Child Development Problems
    • Child Development
    • Developmental concerns in children
    • Abnormal child development
    • Lack of normal development

    ICD-10 Codes:

    • R6250: Unspecified lack of expected normal physiological development in childhood

    Also known as:

    • Mitochondrial Metabolism Disorder
    • MELAS Syndrome
    • Mitochondrial Disease
    • Metabolic Disorder
    • Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
    • Mitochondrial Metabolic Disease
    • Energy Production Disorder
    • Mitochondrial Encephalomyopathy
    • Lactic Acidosis and Stroke-like Episodes

    ICD-10 Codes:

    • E8840: Mitochondrial metabolism disorder, unspecified
    • E8841: MELAS syndrome

    Also known as:

    • Family history of other specified Condition
    • Family History
    • Inherited health risks
    • Genetic predisposition to certain conditions
    • Family history of specific illnesses

    ICD-10 Codes:

    • Z8489: Family history of other specified conditions

    Also known as:

    • Other Metabolic Disorder Screening
    • Health Screening
    • Rare Metabolic Disease Screening
    • Uncommon Metabolic Check

    ICD-10 Codes:

    • Z13228: Encounter for screening for other metabolic disorders

    Also known as:

    • Other Abnormal Findings in Organ or Tissue Samples
    • Unusual Organ Test Results
    • Atypical Tissue Findings
    • Abnormal Specimen Analysis

    ICD-10 Codes:

    • R898: Other abnormal findings in specimens from other organs, systems and tissues

    Also known as:

    • Abnormal Newborn Screening Results
    • Newborn Screening
    • Positive newborn screen
    • Failed newborn screening
    • Newborn test abnormalities

    ICD-10 Codes:

    • P099: Abnormal findings on neonatal screening, unspecified

    Also known as:

    • Infantile Spinal Muscular Atrophy
    • Spinal Muscular Atrophy
    • SMA Type 1
    • Werdnig-Hoffman Disease
    • Severe Infantile SMA

    ICD-10 Codes:

    • G120: Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]

    Also known as:

    • Spinal Muscular Atrophy
    • SMA
    • Progressive Muscle Weakness
    • Motor Neuron Degeneration

    ICD-10 Codes:

    • G129: Spinal muscular atrophy, unspecified

    Also known as:

    • Medium-Chain Acyl-CoA Dehydrogenase Deficiency
    • Lipid Metabolism Disorder
    • Medium-chain acyl-CoA dehydrogenase deficiency
    • MCAD Deficiency
    • Medium-Chain Fatty Acid Oxidation Disorder
    • MCADD

    ICD-10 Codes:

    • E71311: Medium chain acyl CoA dehydrogenase deficiency

    Which procedures does Dr. Champaigne perform as a Clinical Geneticist?

    As a Clinical Geneticist, procedures performed by a Dr. Neena Champaigne may include:

    For detailed information, please contact Dr. Champaigne's office.

    Does Dr. Champaigne accept my insurance?

    Dr. Champaigne accepts most major insurance plans. Important: Please call our office at (843) 792-1414 before your appointment to verify that your specific plan and network are accepted.

    What insurance plans does Dr. Champaigne accept in Charleston, SC?

    Dr. Champaigne in Charleston, SC accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.

    Top Insurances

    • BCBS Unspecified

    • Blue Cross and Blue Shield of North Carolina

    • BlueCross BlueShield of South Carolina

    • Centene

    • Department of Defense / Tricare

    • Independence Blue Cross

    • Medicare

    • Molina

    • State of South Carolina

    • UnitedHealthcare

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    Where is Dr. Champaigne's office located?

    Dr. Neena Champaigne's Primary Practice

    171 Ashley Ave

    Charleston, SC 29425

    (843) 792-1414

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    Dr. Neena Champaigne's Practice 2

    2250 Mall Dr

    North Charleston, SC 29406

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    Dr. Neena Champaigne's Practice 3

    101 Gregor Mendel Cir

    Greenwood, SC 29646

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    What is Dr. Champaigne's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.

    Dr. Champaigne's National Provider Identifier (NPI) number is 1972554897.

    What common questions do patients ask about Dr. Champaigne?

    Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Champaigne

    What is Dr. Neena Champaigne's specialty?

    Dr. Champaigne is a Clinical Geneticist near Charleston, SC. A clinical geneticist is adept at offering thorough diagnostic, management, and counseling services for genetic disorders. Contact Dr. Champaigne to book an appointment today.

    Is this Dr. Neena Champaigne affiliated with a ranked Castle Connolly Top Hospital?

    Yes, Dr. Champaigne is affiliated with Musc Health University Medical Center which is a Castle Connolly Top Hospital. Castle Connolly Top Hospitals are healthcare institutions recognized for their excellence in specific medical procedures and overall patient care. They are identified through a rigorous peer nomination process, evaluating factors like patient outcomes, quality of care, and expertise. The list recognizes hospitals that excel in 20 or more specific medical procedures, representing the top 25% nationwide. Castle Connolly Top Hospitals

    Where can I learn more about Clinical Geneticist?

    Explore Clinical Geneticist with insights from trusted medical experts on EverydayHealth.com, where you'll find the most relevant content and helpful condition guides for up-to date information about symptoms, causes, diagnosis, treatment and more. See all our health guides to find trusted information on medical conditions from our experts at Everyday Health.

    Is Neena Champaigne accepting new patients in Charleston, SC?

    Yes, Dr. Neena Champaigne is accepting new patients at this time.

    Does Dr. Neena Champaigne offer online booking?

    Please contact Dr. Champaigne's office at (843) 792-1414 for information about online booking, telehealth, or to schedule an appointment.

    How can I make an appointment with Neena Champaigne?

    Please contact Dr. Champaigne's office at (843) 792-1414 for information regarding telehealth appointment availability or for scheduling assistance.

    Which board certifications does Dr. Neena Champaigne have?

    Dr. Neena Champaigne is certified by the American Board of Medical Genetics and American Board of Pediatrics.

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