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Table 2 Clinical features of ichthyosis-hypotrichosis syndrome with associated mutations in ST14

From: A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

Mutation

c.3G > A

c.598 + 1G > A

c.1444G > A

(p.D482N)

c.1558G > C

(p.E520Q)

c.2034delG

(p.L678Ffs*84)

c.2269 + 1G > A

c.24791G > A

(p.G827R)

Mutation type

Start codon

Splice site

Missense

Missense

Frameshift

Splice site

Missense

Reference

[7]

[8]

Current report

[4]

[6]

[6]

[5]

Description of ichthyosis

Generalized scaling, sparing flexures

Generalized erythema and scaling, later localized to back

Fine white generalized scale

Fine gray scale sparing elbows and knees

Generalized scaling, sparing flexures and face

Generalized scaling, sparing elbows, knees, and face

Gray to brown generalized scaling, sparing face

Description of hypotrichosis

Light brown, coarse, curly scalp hair, generalized sparse hair including eyebrows, eyelashes

Light brown, receding frontal hairline, partial loss of eyebrows, curled eyelashes

Light brown, coarse scalp hair, recession of frontal hairline, generalized sparse hair

Coarse scalp hair, generalized sparse hair including eyebrows and eyelashes

Light brown, woolly hair, recession of frontal hairline

Sparse scalp, eyebrow, and body hair, with recession of frontal hairline

Curly, light. Sparse, generalized hair

Palmoplantar keratoderma

–

+

–

–

–

–

–

Ocular anomalies

Blepharitis

–

–

–

–

Pinguecula, corneal opacities

Corneal opacities

Dental anomalies

–

–

–

Conical teeth, pitting

–

–

Conical teeth, pitting

Follicular atrophoderma

–

–

+

+

+

+

–

Hypohidrosis

–

–

–

–

+

+

–