SN7
SHORT NOTE
5M
Describe the development of the vertebral column and the limbs.
Development of the Vertebral Column
- Resegmentation is the whole point — it allows the myotome, which remains segmental, to span the joint between two vertebrae and so to move the column
- Without it the muscles would run from the middle of one vertebra to the middle of the same one, and no movement would be possible
Ossification of the Vertebrae
- Three primary centres — one for the centrum and one for each half of the neural arch; appear in the fetal period
- The halves of the arch fuse in the first 3 to 5 years, and with the centrum by about 6 years at the neurocentral joint
- Five secondary centres at puberty — tip of the spine, each transverse process, and two annular epiphyses on the upper and lower surfaces of the body; fuse by about 25 years
Development of the Limbs
- Limb buds appear in week 4 — upper on day 24, lower on day 26; the upper limb is always slightly ahead
- Apical ectodermal ridge (AER) — a thickening of ectoderm at the tip that controls proximodistal growth
- Zone of polarising activity (ZPA) — controls the anteroposterior (thumb to little finger) axis
- Digits are formed by apoptosis of the tissue between the digital rays, in weeks 6 to 8
- The limbs rotate in week 7 — the upper limb laterally 90° and the lower limb medially 90°
Limb Anomalies
| Anomaly | Nature | Note |
|---|---|---|
| Amelia | Complete absence of a limb | — |
| Meromelia / phocomelia | Partial absence; the hand or foot attached close to the trunk | Classically caused by thalidomide, weeks 4–7 |
| Syndactyly | Fused digits — failure of apoptosis between the rays | The commonest limb anomaly |
| Polydactyly | Extra digits | Often familial; seen in Patau syndrome |
| Congenital talipes equinovarus | Club foot | Associated with oligohydramnios and neural tube defects |
| Amniotic band syndrome | Constriction rings or intrauterine amputation | Mechanical, not genetic |
Applied Aspects
- The critical period for the limbs is weeks 4 to 7, which is why thalidomide taken over a few days produced such specific defects depending on exactly when it was taken
- Spina bifida results from failure of the vertebral arches to fuse — the same halves whose ossification is described above
- Hemivertebra — failure of one half of a centrum, causing congenital scoliosis
- Block vertebra — failure of segmentation, with fusion of adjacent vertebrae, as in Klippel–Feil syndrome
- Sacralisation and lumbarisation — transitional vertebrae from shifted boundaries of resegmentation; a common cause of confusion in identifying levels on radiographs, and of low back pain
- Developmental dysplasia of the hip is screened for at birth by the Ortolani and Barlow tests; late diagnosis leads to a permanent limp
All questions in Systemic Embryology
- Q1Describe the development of the heart. Explain the septation of the atria and ventricles and add a note on the congenital anomalies. ★
- Q2Describe the pharyngeal arches with their nerves, muscles and skeletal derivatives. Describe the derivatives of the pharyngeal pouches. ★
- Q3Describe the development of the gastrointestinal tract. Explain the rotation of the midgut and add a note on its anomalies. ★
- Q4Describe the development of the kidney and the urinary bladder. Add a note on the development of the genital ducts. ★
- Q5Describe the development of the face and the palate. Add a note on cleft lip and cleft palate. ★
- SN1Describe the fetal circulation and the changes that occur at birth. ★
- SN2Describe the development of the diaphragm. Add a note on congenital diaphragmatic hernia. ★
- SN3Describe the development of the thyroid gland. Add a note on thyroglossal cyst and ectopic thyroid. ★
- SN4Describe the development of the lungs and the body cavities. ★
- SN5Describe the fate of the vitelline duct. Write in detail on Meckel diverticulum. ★
- SN6Describe the descent of the testis. Add a note on undescended testis and the anomalies of the processus vaginalis. ★
- SN7Describe the development of the vertebral column and the limbs.