
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Pubertal Delay
Introduction
Overview
Overview
Delayed onset of puberty is considered 14 years old in girls and 15 years old in boys. Most frequently, the delay is due to a constitutional, non-pathologic delay in growth and puberty.
Causes
Causes
- Anorexia Nervosa
- Cardiac conditions
- Celiac Sprue
- Chronic infection
- Chronic metabolic disorder
- Chronic Renal Failure
- Cushing syndrome
- Heavy physical excercise
- Hyperprolactinemia
- Hypothyroidism
- Iatrogenic
- Inflammatory Bowel Disease
- Kallmann’s Syndrome
- Kleinfelter’s syndrome (Boys)
- Malignancy
- Malnutrition
- Multiple tropic hormone deficiency
- Noonan’s Syndrome
- Prader-Willi Syndrome
- Somatotropin deficiency
- Turner’s syndrome
Causes by Organ System
Causes in Alphabetical Order
- Addison’s disease
- Adiposogenital dystrophy
- Adrenal failure
- Adrenal hypoplasia congenital
- Alopecia
- Alpha thalassemia
- Anabolic steroids
- Anemia
- Anophthalmia
- Anorchism
- Anorexia nervosa
- Ataxia
- Autoimmune disease
- Autoimmune ovarian failure
- Autoimmune thyroid disease
- Bangstad syndrome
- Bassoe syndrome
- Beta thalassemia
- Biedl-bardet syndrome
- Biemond syndrome type 2
- Bird-headed dwarfism
- Bosma-henkin-christiansen syndrome
- Bulimia nervosa
- Bullous dystrophy
- Camurat-engelmann disease
- Cantu sanchez-corona fragoso syndrome
- Cardiac conditions
- Castration
- Cataract deafness hypogonadism
- Celiac disease
- Celiac sprue
- Central nervous system tumours
- Chemotherapy
- Chondrodysplasia punctata with steroid sulfatase deficiency
- Chromophobe adenoma
- Chromosome 13 ring syndrome
- Chromosome 14 uniparental disomy syndrome
- Chromosome 3, monosomy 3p2
- Chromosome 9, trisomy 9p
- Chronic illness
- Chronic infection
- Chronic metabolic disorder
- Chronic renal failure
- Cockayne syndrome type 1
- Cohen syndrome
- Collagenous celiac disease
- Combined pituitary hormone deficiency
- Congenital adrenal hyperplasia
- Congenital hypopituitarism
- Congenital hypothyroidism
- Congenital spherocytic hemolytic anemia
- Connective-tissue diseases
- Constitutional delay
- Crandall syndrome
- Craniopharyngioma
- Crohn’s disease
- Cushing syndrome
- Cyanotic congenital heart disease
- Cystic fibrosis
- Cytotoxic drugs
- Deafness neurosensory
- Diamond-blackfan anemia
- Ectodermal dysplasia
- Eunuchoidism familial
- Excess thyroid hormone consumption
- Excessive exercise
- Fabry disease
- Familial dysautonomia
- Female reproductive toxicity
- Fibromatosis multiple non ossifying
- Fleisher syndrome
- Forbes disease
- Frasier syndrome
- Froelich’s syndrome
- Fshb mutation
- Germinoma
- Glioma
- Gluten enteropathy
- Glycogen debranching deficiency
- Gonadal dysgenesis epibulbar dermoid
- Gonadotropin deficiency
- Granulomas
- Growth hormone deficiency
- Hall-riggs mental retardation syndrome
- Haspeslagh fryns muelenaere syndrome
- Head trauma
- Heavy physical excercise
- Hersh-podruch-weisskopk syndrome
- Hydrocephalus obesity hypogonadism
- Hyperprolactinemia
- Hyperthyroidism
- Hypogonadism
- Hypogonadotrophic hypogonadism
- Hypopituitarism
- Hypothalamic cyst
- Hypothalamic damage
- Hypothalamic dysfunction
- Hypothalamic infection
- Hypothalamus disease
- Hypothyroidism
- Iatrogenic
- Ichthyosis male hypogonadism
- Image syndrome
- Infantile hypothyroidism
- Infections
- Inflammatory bowel disease
- Insulin-resistance syndrome
- Intrauterine growth retardation
- Isolated gonadotropin deficiency
- Juvenile arthritis
- Kallmann’s syndrome
- Kleinfelter’s syndrome
- Kwashiorkor
- Lack of gonadotrophin-releasing hormone
- Laron pituitary dwarfism
- Laron syndrome
- Laurence-moon-biedl syndrome
- Low body weight
- Luteinizing hormone deficiency
- Lymphangiectasies
- Lymphoedema
- Lyndi’s syndrome
- Malabsorption syndrome
- Malignancy
- Malnutrition
- Malouf syndrome
- Mandibuloacral dysplasia
- Marinesco-sjogren syndrome
- Masculinizing tumor of ovary
- Meningioma
- Mental retardation
- Metaphyseal undermodeling
- Microcephaly
- Mixed gonadal dysgenesis
- Müllerian agenesis
- Multiple tropic hormone deficiency
- Mumps
- Mumps orchitis
- Myopathy
- Neuroectodermal endocrine syndrome
- Niemann-pick disease
- Noonan’s syndrome
- Optic chiasma glioma
- Ovarian cysts
- Ovarian dysgenesis
- Ovarian torsion
- Panhypopituitarism
- Persistent major infection
- Pituitary adenoma
- Pituitary gland abscess
- Pituitary gland cyst
- Pituitary gland damage
- Pituitary gland infection
- Pituitary gland tumor
- Prader-willi syndrome
- Prenatal dwarfism
- Primary gonadal failure
- Prolactinoma
- Pterygia
- Pure dysgenesis
- Pure red cell aplasia
- Radiation therapy
- Refractory celiac disease
- Resistant ovary syndrome
- Retinitis pigmentosa
- Richards-rundle syndrome
- Salti-salem syndrome
- Schaap-taylor-baraitser syndrome
- Schofer beetz bohl syndrome
- Sengers-hamel-otten syndrome
- Serious emotional stress
- Serious ovarian infection
- Serious testicular infection
- Shprintzen-golberg craniosynostosis
- Sickle cell anemia
- Singh-chhaparwal-dhanda syndrome
- Sohval-soffer syndrome
- Somatotropin deficiency
- Spastic paraplegia with kallmann syndrome
- Spinocerebellar ataxia
- Thyroid agenesis
- Torsion of the testis
- Trauma
- Tricho-hepato-enteric syndrome
- Tuberculosis
- Turner’s syndrome
- Type 1 diabetes
- Type iii glycogen storage disease
- Ulnar-mammary syndrome of pallister
- Underactive thyroid gland
- Undescended testes
- Vascular lesions
- William’s syndrome
- Woodhouse sakati syndrome
- X-irradiation
- Zinc deficiency
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Luke Rusowicz-Orazem, B.S.
