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Pichler, R; Stelzer, C; Berg, J; Holzinger, C; Eckl, KM; Hennies, HC; Auböck, J.
Hypoplastic thyroid, growth hormone deficiency, corneal opacities, cataract and hyperkeratotic skin disease: a possible new ichthyosis syndrome associated with endocrinopathies.
Arch Dermatol Res. 2005; 296(12):585-587 Doi: 10.1007/s00403-005-0566-8 (- Case Report)
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Führende Autor*innen der Med Uni Graz
Pichler Robert
Co-Autor*innen der Med Uni Graz
Berg Jörg
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Abstract:
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.
Find related publications in this database (using NLM MeSH Indexing)
Cataract - etiology
Corneal Opacity - etiology
Human Growth Hormone - deficiency
Humans -
Hypothyroidism - etiology
Ichthyosis Vulgaris - complications Ichthyosis Vulgaris - genetics
Keratosis - etiology
Male -
Middle Aged -
Syndrome -
Thyroid Gland - pathology

Find related publications in this database (Keywords)
ichthyosis syndrome
hypothyroidism
growth hormone deficiency
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