Skull

With the lemon sign, the frontal bones are flattened (almost concave) so that the anterior skull is not as rounded.

What our notes say

Study material on Skull

Images

Q43 - sagittal MRI of the lower spine showing a mass
Q43 - sagittal MRI of the lower spine showing a mass
Sagittal embryo section with neural tube cross-sections labelled A, B, C
Sagittal embryo section with neural tube cross-sections labelled A, B, C
Four clinical photos of infants with skull/facial anomalies A, B, C, D
Four clinical photos of infants with skull/facial anomalies A, B, C, D
Coronal section through the scalp and meninges with X, A, B, C, D labelled
Coronal section through the scalp and meninges with X, A, B, C, D labelled
Sagittal skull illustration with dural venous sinuses A, B, C, D labelled
Sagittal skull illustration with dural venous sinuses A, B, C, D labelled
Two clinical photos: A, thickened scaly skin over the knees; B, a man with excessive body and facial hair
Two clinical photos: A, thickened scaly skin over the knees; B, a man with excessive body and facial hair
Base of skull, anterior cranial fossa with A, B, C labelled
Base of skull, anterior cranial fossa with A, B, C labelled
Infant skull showing fontanelles A, B and facial prominences C, D
Infant skull showing fontanelles A, B and facial prominences C, D

Practice questions on Skull

A 72-year-old man presents with back pain and confusion. X-ray shows punched-out lytic skull lesions. Serum electrophoresis shows an IgG M protein spike. Urine shows Bence Jones proteins. Bone marrow has >30% plasma cells. Creatinine is markedly elevated. Which mechanism BEST explains his renal dysfunction?

Answer: C. This is multiple myeloma. Renal dysfunction results primarily from obstructive proteinaceous casts — composed mostly of Bence Jones proteins (free light chains) along with Tamm-Horsfall protein and albumin — forming in the distal convoluted tubules and collecting ducts. Adjacent epithelial cells become necrotic from the toxic effects of Bence Jones proteins. It is hypercalcaemia (not hypocalcaemia) that also contribu

Which of the following is MOST CORRECT regarding the formation of the skull?

Answer: C. ** The skull base develops from both neural crest cells and paraxial mesoderm, and both undergo endochondral ossification. The calvarium undergoes intramembranous ossification. --- ---

A port wine stain in the distribution of the trigeminal nerve is found in a child with seizures, intellectual disability, and skull "tram-track" calcifications. What underlying mutation causes this syndrome?

Answer: D. Sturge-Weber syndrome (port wine stain + leptomeningeal angiomas + seizures + intellectual disability) is caused by a somatic GNAQ missense mutation occurring early in development — not inherited. ---

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