Referral Guidelines are peer reviewed guidelines developed to assist referring providers in their approach to a patient presenting with common signs or symptoms suggestive of an endocrine condition, and when to refer to Pediatric Endocrinology.
Females before 8 yrs of age:
Estrogenic: Breast development, vaginal discharge/bleeding
Androgenic: Pubic hair, axillary hair body odor, acne
Males before 9 yrs of age:
Testicular enlargement, pubic hair, axillary hair, body odor, acne
For both sexes:
Growth acceleration, exposure to exogenous hormones, history of brain injury or radiation, family history of early puberty, midline defects, severe hypothyroidism, café au lait macules, FH/history of neurofibromatosis
Refer to Differential Diagnosis section
Radiological tests:
- Bone age
Blood tests:
- LH*
- FSH*
- testosterone (males)*
- estradiol (females)*
- DHEA-S
- TSH
- Free T4
*Pubertal laboratory tests should be obtained in the early AM using sensitive pediatric assays only
Other tests to consider after consultation with Pediatric Endocrinology:
- 17-OH progesterone
- androstenedione
- Pelvic ultrasound
- Brain MRI
Urgent:
- CNS abnormality such as headaches, seizures or visual changes
- very elevated 17-OH progesterone
- rapidly progressing puberty
- very young age
- initial presentation is vaginal bleeding
- Bone age greater than 2 SD above chronologic age
- signs of rapid virilization
Routine: Normal bone age, normal labs
- Previous growth data/growth charts
- Pertinent medical records
- Recent laboratory and radiologic studies (including image of bone age)
- Idiopathic (80% of cases in females, 10% of cases in males)
- CNS lesion
- Hypothalamic Hamartoma
- Other CNS tumors or lesions
- Genetic abnormality
- Gain-of-function mutation of the G-protein-coupled kisspeptin-1 receptor (GPR54)
- Sex-steroid exposure causing bone age advancement
Gonadotropin-independent sexual precocity
- Normal variants
- Premature thelarche
- Premature adrenarche
- Neuroendocrine
- LH/hCG excess
- Hypothyroidism
- Adrenal
- Congenital adrenal hyperplasia
- Adrenal tumor
- Gonadal
- McCune-Albright Syndrome
- Leydig cell tumor
- Ovarian tumor
Familial male-limited precocious puberty (testotoxicosis)
Gad B. Kletter, Karen O. Klein, Yolanda Y. Wong . A pediatrician's guide to central precocious puberty. Clinical Pediatrics 2015 May; 54(5):414-24
Author: Deanna Adkins
Reviewed 12/2022 by Michelle Knoll
