Accepting patients
Who is Dr. Pereira, Clinical Geneticist in New York, NY?
Dr. Elaine Pereira is a Clinical Geneticist, who primarily practices in New York, NY with 2 additional practice locations. She is board certified. Dr. Pereira graduated from Albert Einstein and completed her residency at Montefiore Medical Center. Dr. Pereira is fluent in English, and is currently seeing new patients. To book an appointment or to confirm insurance options, please call Dr. Pereira’s office at (718) 741-2323.
Where did Dr. Pereira go to medical school and complete their residency?
Residency: Montefiore Medical Center
Medical School: Albert Einstein | Albert Einstein College of Medicine of Yeshiva University
Is Dr. Pereira board certified as a Clinical Geneticist?
Yes, Dr. Elaine Pereira is board certified by the American Board of Pediatrics , American Board of Medical Genetics since 2013, American Board of Pediatrics since 2010
What languages does Dr. Pereira speak?
Dr. Pereira and their clinical team can communicate with patients in the following languages:
English
What conditions does Dr. Pereira treat?
As a Clinical Geneticist, Dr. Pereira 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. Pereira. 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:
- Autism
- Autism Spectrum Disorder
- Classic Autism', 'Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
Also known as:
- Chromosomal Abnormality
- 22q11.2 Deletion Syndrome
- Other Chromosomal Abnormality
- Extra Chromosome
- Autosomal Deletion Syndrome
- Genetic Disorder
- 22q11.2 deletion syndrome
- Genetic Chromosome Disorder
- Chromosome Problem
- Aneuploidy
- Velo-Cardio-Facial Syndrome
- DiGeorge Syndrome
- Catch 22 Syndrome
- Rare Chromosome Disorder
- Atypical Chromosomal Condition
- Genetic Chromosome Problem
- Trisomy
- Partial Trisomy
- Autosomal Trisomy
- Autosomal Microdeletion
- Chromosome Deletion
- Genetic Deletion
ICD-10 Codes:
- Q999: Chromosomal abnormality, unspecified
- Q9381: Velo-cardio-facial syndrome
- Q998: Other specified chromosome abnormalities
- Q928: Other specified trisomies and partial trisomies of autosomes
- Q9389: Other deletions from the autosomes
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:
- Sensorineural Hearing Loss
- Hearing Disorder and Deafness
- Nonsyndromic hearing loss
- Nerve Deafness
- Inner Ear Hearing Loss
- SNHL
- Permanent Hearing Loss
ICD-10 Codes:
- H903: Sensorineural hearing loss, bilateral
Also known as:
- Other Genetic Syndrome
- Birth Defects Causing Overgrowth
- Birth Defects
- Rare Birth Defect Syndromes
- Uncommon Congenital Syndromes
- Overgrowth Syndromes
- Congenital Gigantism
ICD-10 Codes:
- Q8789: Other specified congenital malformation syndromes, not elsewhere classified
- Q873: Congenital malformation syndromes involving early overgrowth
Also known as:
- Cafe-au-lait Spots
- Birthmarks
- CALMs
- Coffee-with-Milk Spots
- Light Brown Birthmarks
ICD-10 Codes:
- L813: Cafe au lait spots
Also known as:
- Family History of Heart Disease
- Family History
- Heart Disease
- Hereditary heart disease risk
- Genetic predisposition to heart problems
- Heart conditions in the family
ICD-10 Codes:
- Z8249: Family history of ischemic heart disease and other diseases of the circulatory system
Also known as:
- Developmental Speech and Language Disorder
- Speech and Communication Disorder
- Childhood Language Delay
- Global Speech Delay
- Unspecified Communication Disorder
ICD-10 Codes:
- F809: Developmental disorder of speech and language, unspecified
Also known as:
- Failure to Thrive in Children
- Short Stature in Children
- Growth Disorder
- Poor growth in children
- Childhood growth problems
- Infant growth failure
- Child Growth Problems
- Dwarfism
- Growth Retardation
ICD-10 Codes:
- R6251: Failure to thrive (child)
- R6252: Short stature (child)
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:
- Seizures
- Epilepsy
- Convulsions
- Fits
ICD-10 Codes:
- R569: Unspecified convulsions
Also known as:
- Family History of Birth Defects or Genetic Disorder
- Birth Defects
- Family History
- Genetic Disorder
- Genetic risk for birth defects
- Hereditary chromosomal abnormalities
- Congenital anomalies in family
ICD-10 Codes:
- Z8279: Family history of other congenital malformations, deformations and chromosomal abnormalities
Also known as:
- Down Syndrome
- Trisomy 21
- Mongolism
ICD-10 Codes:
- Q909: Down syndrome, unspecified
Also known as:
- Neurofibromatosis Type 1
- Neurofibromatosis
- Neurofibromatosis type 1
- NF1
- Von Recklinghausen disease
- Peripheral neurofibromatosis
ICD-10 Codes:
- Q8501: Neurofibromatosis, type 1
Which procedures does Dr. Pereira perform as a Clinical Geneticist?
As a Clinical Geneticist, procedures performed by Dr. Elaine Pereira may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Pereira's office.
Does Dr. Pereira accept my insurance?
Please contact Dr. Pereira's office to confirm accepted insurance plans.
Where is Dr. Pereira's office located?
Dr. Elaine Pereira's Primary Practice
3959 Broadway # 718
New York, NY 10032
(718) 741-2323
What is Dr. Pereira's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Pereira's National Provider Identifier (NPI) number is 1578841557.
What common questions do patients ask about Dr. Pereira?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Pereira
What is Dr. Elaine Pereira's specialty?
Dr. Pereira is a Clinical Geneticist near New York, NY. A clinical geneticist is adept at offering thorough diagnostic, management, and counseling services for genetic disorders. Contact Dr. Pereira to book an appointment today.
Is this Dr. Elaine Pereira affiliated with a ranked Castle Connolly Top Hospital?
No, Pereira is not affiliated with a Castle Connolly Top Hospital. Castle Connolly Top Hospitals 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 Elaine Pereira accepting new patients in New York, NY?
Yes, Dr. Elaine Pereira is accepting new patients at this time.
Does Dr. Elaine Pereira offer online booking?
Please contact Dr. Pereira's office at (718) 741-2323 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Elaine Pereira?
Please contact Dr. Pereira's office at (718) 741-2323 for information regarding telehealth appointment availability or for scheduling assistance.
Which board certifications does Dr. Elaine Pereira have?
Dr. Elaine Pereira is certified by the American Board of Pediatrics and American Board of Medical Genetics.
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