Menkes syndrome - Hair and Scalp
Menkes syndrome is characterized by hair shaft abnormalities and hypopigmentation of the skin and hair. The most common hair shaft finding is pili torti (twisted hairs, corkscrew hairs), but other hair defects, including trichorrhexis nodosa and monilethrix, have been reported. Connective tissue alterations include skin and joint laxity, osteoporosis, arterial abnormalities, and bladder diverticula. Progressive neurodegenerative consequences are devastating and typically begin with progressive hypotonia, loss of social interaction, and subsequent severe intellectual disability. The disease is caused by a mutation in a transporting ATPase that functions to transfer copper into copper-dependent enzymes. Copper thus accumulates in the intestine and renal glomerulus but cannot be transported to target organs.
Although patients are born without complications, by 2-3 months of life, hair abnormalities can be seen, characterized by short, sparse, depigmented hair. Subsequent neurological deterioration and other connective tissue manifestations also become apparent by this age.
Diagnosis is confirmed by low serum copper and ceruloplasmin levels. Most patients who do not receive treatment die by age 3, and those who do receive therapy typically die by age 10. Death is usually due to complications from neurological deterioration and organ failure.
Milder variants of Menkes syndrome exist, including mild Menkes syndrome and occipital horn syndrome (OHS). These syndromes arise from mutations in the Menkes genetic locus that permit residual enzyme function.
Treatment of Menkes syndrome relies on intervenously or subcutaneously administered copper supplementation. However, if initiation of this therapy begins after 2 months of age, the neurodegenerative consequences cannot be prevented. In those infants where treatment was initiated in the immediate newborn period, some have had improved neurologic outcome, with only modest deficits, whereas others have not had profound improvement.
For more information, see OMIM.
E83.09 – Other disorders of copper metabolism
59178007 – Menkes kinky-hair syndrome
- Bjornstad syndrome
- Crandall syndrome
- Mitochondrial disorders
- Netherton syndrome
- Bazex-Dupré-Christol syndrome
- Laron syndrome
- Child abuse (eg, traumatic alopecia) – may be considered in circumstance of multiple fractures
- Other disorders of neurological deterioration, metabolic disorders, or enzyme deficiencies.