Low, D., Tang, M.M., Surana, U., Lee, J.Y., Pramano, Z.A.D. and Leong, K.F. (2019), H syndrome – the first report in Malaysia. Int J Dermatol, 58: e190-e193. doi:10.1111/ijd.14518
Abstract:
H syndrome (OMIM #612391) is a rare autosomal recessive disorder, first described by Molho-Pessach et al1 for the common clinical features of hyperpigmentation, hypertrichosis, hepatosplenomegaly, hearing loss, heart anomalies, hypogonadism, low height, hyperglycemia (insulin-dependent diabetes mellitus), and hallux valgus/flexion contractures. Here we described the first confirmed case of H syndrome of Indian ethnicity in
Malaysia.
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PublisherCopyrights
Funding Info:
Source of funding: Paediatric Institute, Hospital Kuala Lumpur, Malaysia.
Description:
This is the peer reviewed version of the following article: Low, D., Tang, M.M., Surana, U., Lee, J.Y., Pramano, Z.A.D. and Leong, K.F. (2019), H syndrome – the first report in Malaysia. Int J Dermatol, 58: e190-e193. doi:10.1111/ijd.14518, which has been published in final form at https://doi.org/10.1111/ijd.14518. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.