We are part of multidisciplinary groups providing comprehensive care for patients with Turner syndrome, Klinefelter syndrome and Williams syndrome, and serve as consultants for patients with Down syndrome, Prader-Willi syndrome and other genetic conditions with endocrine implications.

We treat short stature and/or endocrine disorders in genetic conditions such as:

  • Turner syndrome
  • Klinefelter syndrome
  • Kallman syndrome and other genetic conditions causing hypogonadotropic hypogonadism
  • Genetic conditions causing differences of sexual development
  • Genetic conditions causing hypopituitarism or predisposing patients to develop pituitary tumors
  • Carney complex
  • Multiple endocrine neoplasia 1 and 2
  • Polyglandular autoimmune syndromes
  • McCune Albright syndrome
  • Familial male limited precocious puberty
  • Congenital adrenal hyperplasia
  • Muscular dystrophy (Duchenne’s muscular dystrophy and spinal muscular atrophy)
  • Osteogenesis imperfecta and other genetic conditions involving bone
  • Genetic conditions involving calcium and phosphorus metabolism
  • Williams syndrome
  • 2 deletion syndrome
  • Down syndrome
  • Prader-Willi syndrome
  • Silver-Russell syndrome
  • Noonan syndrome
  • Cystic fibrosis related diabetes
  • Maturity Onset Diabetes of the Young (MODY)
  • Genetic causes of obesity
  • Hyperinsulinemic hypoglycemia of infancy