Experienced in Ectodermal Dysplasias
Experienced in Ectodermal Dysplasias
3400 Civic Center Boulevard, South Pavilion, 1st Floor, 
Philadelphia, PA 

Overview

Staci Kallish is a Medical Genetics provider in Philadelphia, Pennsylvania. Dr. Kallish is rated as an Experienced provider by MediFind in the treatment of Ectodermal Dysplasias. Her top areas of expertise are Neurofibromatosis Type 1 (NF1), Gaucher Disease Type 1, Fabry Disease, and Neurofibromatosis. Dr. Kallish is currently accepting new patients.

Her clinical research consists of co-authoring 21 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 1 article in the study of Ectodermal Dysplasias.

Graduate Institution
University Of Medicine And Dentistry Of New Jersey, School Of Osteopathic Medicine
Residency
Cooper University Hospital
Specialties
Medical Genetics
Licenses
Clinical Biochemical Genetics in PA
Board Certifications
Clinical Genetics And Genomics, 2022
Med Genetics/Clinical Biochem (AMA)Pediatrics, 2008
Fellowships
Children's Hospital of Philadelphia
Hospital Affiliations
Hospital Of Univ Of Pennsylvania
Languages Spoken
English
Gender
Female

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Accepted insurance plans:

Aetna
  • EPO
  • HMO
  • POS
  • PPO
Blue Cross Blue Shield
  • EPO
  • HMO
  • POS
  • PPO
Cigna
  • EPO
  • HMO
  • PPO
Clover Health
  • INSURANCE PLAN
  • MEDICARE MAPD
Devoted Health
  • MEDICARE MAPD
  • OTHER MEDICARE
Geisinger
  • HMO
  • POS
  • PPO
Highmark
  • EPO
  • HMO
  • PPO
Horizon Healthcare
  • EPO
  • POS
Humana
  • HMO
  • INDEMNITY
  • POS
  • PPO
Independent Health
  • EPO
  • POS
  • PPO
Medicare
  • INSURANCE PLAN
  • MANAGED MEDICAID PLAN
  • MEDICARE MAPD
  • MEDICARE PDP
  • MEDICARE SNP
  • MEDICARE-MEDICAID PLAN
  • OTHER MEDICARE PART D
Oscar
  • EPO
  • HMO
  • PPO
Provider Partners Health Plan
  • MEDICARE SNP
UnitedHealthcare
  • EPO
  • HMO
  • POS
  • PPO
UPMC
  • EPO
  • PPO
View 10 Less Insurance Carriers -

Locations

Penn Translational Medicine and Human Genetics
3400 Civic Center Boulevard, South Pavilion, 1st Floor, Philadelphia, PA 19104

Additional Areas of Focus

Dr. Kallish has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.

Fragile X Syndrome
Idiopathic Pulmonary Fibrosis
Aortic Dissection
Beckwith-Wiedemann Syndrome
Kallmann Syndrome
Holt-Oram Syndrome
Albinism
Interstitial Lung Disease
Alport Syndrome
Craniosynostosis
Marfan Syndrome
Gaucher Disease
Angelman Syndrome
Hypogonadotropic Hypogonadism
Turner Syndrome
Aarskog Syndrome
Klinefelter Syndrome
Alkaptonuria
Alagille Syndrome
Incontinentia Pigmenti
Dyskeratosis Congenita
Cornelia De Lange Syndrome
Fabry Disease
Neurofibromatosis Type 1 (NF1)
Polycystic Kidney Disease
Moyamoya Disease
View 16 Less Areas of Focus-

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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Alanna Strong is a Medical Genetics specialist and a Pediatrics provider in Philadelphia, Pennsylvania. Dr. Strong is rated as a Distinguished provider by MediFind in the treatment of Ectodermal Dysplasias. Her top areas of expertise are Hardikar Syndrome, Aplasia Cutis Congenita, Ectodermal Dysplasias, and Clouston Syndrome.

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.

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