Cerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndrome

CEDNIK syndrome is a rare congenital condition that presents as severe developmental failure of the nervous system and the epidermis. Clinical manifestations include microcephaly, cerebral dysgenesis, facial dysmorphism, palmoplantar keratoderma, and ichthyosis.[3]

These children usually have a normal intauterine life and normal birth. The first symptoms to appear are abnormal eye movements, poor head and trunk control and failure to thrive. The facial dysmorphism is characteristic with elongated faces, antimongolian eye slant, slight hypertelorism and flat broad nasal root. Palmoplantar keratoderma and ichthyosis appeares between 5 and 11 months of age.Soon features of psychomotor retardation as seen as a delay in major developmental milestones, becomes evident.Severe peripheral neuropathy is common in these children. Early macular degeneration is yet another clinical feature.[4] Death is common by 5–10 years and is usually as a result of infection or aspiration pneumonia.

Tendon reflexes are usually absent.Nerve conduction studies usually show decreased amplitude indicating decrease in the number of active neurons.Muscle biopsies show atrophic changes.

Ophthalmologic evaluation show hypoplastic optic disk and electrophysiological studies were suggestive of decreased conductance in retina and features of macular atrophy.

Mild sensorineural deafness is seen.

Brain MRI show abnormal of corpus callosum and cortical dysplasia, with pachygyria and polimicrogyria .

This condition is associated with a loss-of-function mutation in SNAP29 gene, encoding a member of the SNARE family of proteins which is involved in intracellular vesicle fusion .Decrease in SNAP29 expression was found to result in abnormal lamellar granule maturation and secretion.[5] Lamellar granules are organelles found in the upper epidermal layers of skin and is responsible for secretion of lipids, proteases and their inhibitors to stratum corneum during the formation of epidermal barrier.Due to the abnormal vesicle trafficking as a consequence of decreased SNAP29 there is abnormal deposition of epidermal lipids and proteases.[4]

The abnormal gene of CEDNIK disease was mapped on chromosome 22 by Sprecher E et al.[4]

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