Constitutional growth delay

Last updated: November 01, 2022

Constitutional growth delay

Exam 1 -AHN 548 -

Exam 1 -AHN 548 -

Anatomy of the breast
Anatomy clinical correlates: Breast
Mammary gland histology
Ovary histology
Fallopian tube and uterus histology
Cervix and vagina histology
Anatomy and physiology of the female reproductive system
Puberty and Tanner staging
Estrogen and progesterone
Menstrual cycle
Menopause
Pregnancy
Oxytocin and prolactin
Breastfeeding
Stages of labor
Precocious puberty
Delayed puberty
Klinefelter syndrome
Turner syndrome
5-alpha-reductase deficiency
Androgen insensitivity syndrome
Kallmann syndrome
Amenorrhea
Ovarian cyst
Premature ovarian failure
Ovarian torsion
Polycystic ovary syndrome
Krukenberg tumor
Ovarian sex-cord stromal tumors
Ovarian surface epithelial tumors
Ovarian germ cell tumors
Uterine fibroid
Endometriosis
Endometritis
Endometrial hyperplasia
Choriocarcinoma
Endometrial cancer
Cervical cancer
Pelvic inflammatory disease
Urethritis
Mastitis
Fibrocystic breast changes
Phyllodes tumor
Intraductal papilloma
Paget disease of the breast
Breast cancer
Gestational hypertension
Hyperemesis gravidarum
Preeclampsia & eclampsia
Gestational diabetes
Placenta previa
Placenta previa
Cervical incompetence
Placenta accreta
Placental abruption
Oligohydramnios
Polyhydramnios
Potter sequence
Intrauterine growth restriction
Preterm labor
Postpartum hemorrhage
Chorioamnionitis
Congenital toxoplasmosis
Congenital syphilis
Congenital cytomegalovirus (NORD)
Neonatal conjunctivitis
Neonatal herpes simplex
Neonatal sepsis
Congenital rubella syndrome
Neonatal meningitis
Miscarriage
Gestational trophoblastic disease
Ectopic pregnancy
Fetal alcohol syndrome
Uterine disorders: Pathology review
Cervical cancer: Pathology review
Benign breast conditions: Pathology review
Ovarian cysts and tumors: Pathology review
Vaginal and vulvar disorders: Pathology review
Breast cancer: Pathology review
Complications during pregnancy: Pathology review
Congenital TORCH infections: Pathology review
Amenorrhea: Pathology review
Estrogens and antiestrogens
Androgens and antiandrogens
Uterine stimulants and relaxants
Progestins and antiprogestins
Aromatase inhibitors
Prolactinoma
Breast cancer: Clinical
Abnormal uterine bleeding: Clinical
Cervical cancer: Clinical
Genito-pelvic pain and penetration disorder
Sexual dysfunctions: Clinical
Infertility: Clinical
Amenorrhea: Clinical
Contraception: Clinical
Physical and sexual abuse
Sexual orientation and gender identity
Female sexual interest and arousal disorder
Orgasmic dysfunction
Ovarian cysts, cancer, and other adnexal masses: Clinical
Vulvovaginitis: Clinical
Hypertensive disorders of pregnancy: Clinical
Perinatal infections: Clinical
Gestational trophoblastic disease: Clinical
Routine prenatal care: Clinical
Abnormal labor: Clinical
Neonatal jaundice: Clinical
Streptococcus agalactiae (Group B Strep)
Neonatal hepatitis
Neonatal respiratory distress syndrome
Jaundice
Jaundice: Clinical
Enuresis
Nocturnal enuresis
Elimination disorders: Clinical
Biliary colic
Night terrors
ADHD: Information for patients and families (The Primary School)
Attention deficit hyperactivity disorder
Autism spectrum disorder
Fragile X syndrome
Precocious and delayed puberty: Clinical
Constitutional growth delay
Inheritance patterns
Mendelian genetics and punnett squares
Mitochondrial myopathy
Body dysmorphic disorder
Down syndrome (Trisomy 21)
Edwards syndrome (Trisomy 18)
Patau syndrome (Trisomy 13)
Cri du chat syndrome
DiGeorge syndrome
Williams syndrome
Neurofibromatosis
Marfan syndrome
Achondroplasia
Osteogenesis imperfecta
Craniosynostosis
Myelodysplastic syndromes
Cystic fibrosis
Cystic fibrosis: Pathology review
Cystic fibrosis: Clinical
Alport syndrome
Spinal muscular atrophy
Muscular dystrophy
Hemophilia
Prader-Willi syndrome
Angelman syndrome
Beckwith-Wiedemann syndrome
Acute intermittent porphyria
Familial hypercholesterolemia
Gaucher disease (NORD)
Cleft lip and palate
Spina bifida
Developmental milestones: Clinical

Flashcards

Constitutional growth delay

0 of 6 complete

Questions

USMLE® Step 1 style questions USMLE

0 of 1 complete

A 12-year-old boy is brought to the physician for evaluation. During evaluation of sexual development of the boy, his genitalia and pubic hair are at Tanner stage 2 of sexual development. Which of the following characteristics are expected to be seen at this stage of sexual development?  

Transcript

Watch video only

Constitutional growth delay is a normal variation of development where there’s a temporary delay in growth that occurs during early childhood and puberty.

You can think of it as a slowed rate of maturation, which happens normally in some people.

It’s the most common cause of short stature and pubertal delay in children and adolescents, but by adulthood, people with constitutional growth delay generally end up with normal adult heights.

Generally speaking, there are two hormonal systems that control growth - the growth hormone axis and the hypothalamic-pituitary-gonadal axis.

The growth hormone axis starts with the hypothalamus which is at the base of the brain.

The hypothalamus secretes growth hormone-releasing hormone and that stimulates the anterior pituitary gland to produce growth hormone.

Now, growth hormone affects lots of tissues - in particular it makes the body retains nitrogen leading to more muscle growth, and osteoblasts get stimulated which causes the bones to thicken.

Growth hormone also stimulates certain tissues like the liver, skeletal muscles, bones, and kidneys to produce somatomedin C, also called insulin-like growth factor 1.

Insulin-like growth factor 1 promotes cellular metabolism, prevents cell death, and helps cell divide and differentiate throughout the body.

It’s also the key hormone that stimulates the growth in length of long bones.

Now, sexual maturation is under the control of the hypothalamic-pituitary-gonadal axis.

This axis also starts with the hypothalamus which releases Gonadotropin-releasing hormone, or GnRH which stimulates the anterior pituitary to produce the gonadotropin hormones: luteinizing hormone, or LH, and follicle-stimulating hormone, or FSH.

LH and FSH stimulate the gonads to produce sex specific hormones - which are estrogen and progesterone in females, and testosterone in males.

Now, the amount of hormone that gets produced by this axis varies over a person’s lifetime, and that affects the development of the sex organs, as well as the appearance of secondary sexual characteristics.

During puberty, there’s increased GnRH production and increased levels of FSH and LH, and that triggers the onset of sexual maturity.

The stages of sexual maturity that a person goes through are referred to as the Tanner scale.

The Tanner scale centers on two, independent criteria: the appearance of pubic hair in both sexes; and the increase in testicular volume and penile size and length in males, and breast development in females.

There are five stages: In stage 1, the prepubertal stage, no pubic hair is present in either sex.

Males have a small penis and testes. Females have a flat-chest.

In stage 2, pubic hair appears and there’s a measurable enlargement of the testes; and breast buds appear.

In stage 3, pubic hair becomes coarser; the penis begins to enlarge in both size and length; and breast mounds form.

In stage 4, pubic hair begins to cover the pubic area; the penis begins to widen; and breast enlargement continues to form something called a “mound-on-mound” contour.

In stage 5, pubic hair extends to the inner thigh; the penis and testes have enlarged to adult size; and the breast takes on an adult contour.

Constitutional growth delay is not a disorder but a normal variation in the rate of growth.

Growth charts are often used to track the development of children, and they usually have age on the X, or horizontal axis and head circumference, weight, or height on the Y, or vertical axis.

The children typically have normal height and weight at birth but during the first few years of life their growth rate declines.

Key Takeaways

Constitutional growth delay (CGD) is a condition in which some children grow slowly during early childhood and puberty compared to their peers. CGD is the most common cause of short stature in children and pubertal delay in adolescents. It is considered a normal variation to growth because individuals with constitutional growth delay usually end up achieving normal adult heights by adulthood.

Sources

  1. "Robbins Basic Pathology" Elsevier (2017)
  2. "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
  3. "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
  4. "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
  5. "Harrison's Endocrinology, 4E" McGraw-Hill Education / Medical (2016)
  6. "Recent advances in the understanding and management of delayed puberty" Archives of Disease in Childhood (2015)
  7. "Constitutional delay of puberty versus congenital hypogonadotropic hypogonadism: Genetics, management and updates" Best Practice & Research Clinical Endocrinology & Metabolism (2019)