Conditions We Treat

We are following children with the following syndromes and conditions:

Ataxia-Telangectasia
Beckwith-Wiedemann Syndrome / Isolated Hemihypertrophy
Bannayan-Riley-Ruvalcaba Syndrome
Biallelic mismatch repair gene mutations
Costello Syndrome
Cowden Syndrome
Denys-Drash
DICER1-related Pleuropulmonary Blastoma Family Tumor and Dysplasia Syndrome
Familial Adenomatous Polyposis
Hereditary Leiomyomatosis and Renal Cell Cancer
Hereditary Paraganglioma-Pheochromocytoma Syndrome
Li-Fraumeni Syndrome
Multiple Endocrine Neoplasia, Type 1
Multiple Endocrine Neoplasia, Type 2
Nevoid Basal Cell Carcinoma (Gorlin) Syndrome
Peutz-Jeghers Syndrome
Rhabdoid Predisposition Syndrome
Simpson-Golabi-Behmel
Tuberous Sclerosis Complex
Von Hippel-Lindau Disease
WAGR
Paraneoplastic syndromes with concern for occult malignancy
Other rare syndromes/conditions in which cancer risk is greatly elevated and screening may improve outcomes