Dr. Ian D Krantz M.D.
Pediatrician
34th & Civic Center Blvd Children's Hospital Philadelphia PA, 19104About
Dr. Ian Krantz is a pediatrician practicing in Philadelphia, PA. Dr. Krantz is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Krantz diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Krantz can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
Tel Aviv Univ- Sackler Fac Of Med- Tel Aviv- Israel 1991
Tel Aviv University / Sackler Faculty of Medicine 1991
Sackler School of Medicine 1991
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Clinical and molecular genetics of Alagille syndrome.
- Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypes.
- Jagged1 mutations in alagille syndrome.
- Chromosomal localization, genomic characterization, and mapping to the Noonan syndrome critical region of the human Deltex (DTX1) gene.
- Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients.
- Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange syndrome.
- Dominant paternal transmission of Cornelia de Lange syndrome: a new case and review of 25 previously reported familial recurrences.
- Homozygosity for the V37I Connexin 26 mutation in three unrelated children with sensorineural hearing loss.
- Alagille syndrome: chipping away at the tip of the iceberg.
- Facial features in Alagille syndrome: specific or cholestasis facies?
- Supernumerary digital flexion creases: an additional clinical manifestation of Alagille syndrome.
- Craniosynostosis in Alagille syndrome.
- Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletion.
- Consequences of JAG1 mutations.
Treatments
- Hearing Loss
- Epilepsy
- Learning Disabilities
- Birth Defects
- Congenital Heart Disease
- Malnutrition
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