Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: A possible new ichthyosis syndrome associated with endocrinopathies

Robert Pichler, Christoph Stelzer, Jörg Berg, Carl Holzinger, Katja Martina Eckl, Hans Christian Hennies, Josef Auböck

Research output: Contribution to journalArticle

3 Citations (Scopus)


A 56 year old man presented with ichthyosis vulgaris since early childhood, clinically characterised by fine scaling of the trunk and hyperkeratotic scales on the exterior surfaces of the upper and lower extremities. The patient also showed hypothyroidism due to hypoplastic thyroid, cataract, hypercholesterinemia with concommitant arcus cornealis and biliary concrements. Renal lithiasis caused by calcio-oxalate was additionally present. Endocrinological screening revealed growth hormone deficiency in the 1.55 m tall man-(secondary) osteoporosis was observed. The clinical symptomatology indicates that this case cannot be considered as a subtype of the inherited ichthyosis group, but suggests a new syndrome as a separate nosologic entity.

Original languageEnglish
Pages (from-to)585-587
Number of pages3
JournalArchives of Dermatological Research
Issue number12
Publication statusPublished - Jun 2005
Externally publishedYes


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