SHOX (short stature homeobox-containing gene) is the first gene that has been shown to be relevant to the development of specific features in Turner's syndrome. This article reviews clinical findings in patients with SHOX haploinsufficiency caused by intragenic mutations, pseudoautosomal submicroscopic deletions, and cytogenetically recognizable Xp deletions. SHOX haploinsufficiency can result in not only short stature but also Turner skeletal features, such as cubitus valgus, short metacarpals, Madelung deformity, Léri-Weill dyschondrosteosis, high arched palate, and short neck. Rare Turner skeletal features such as Madelung deformity and Léri-Weill dyschondrosteosis are primarily facilitated by the bone-maturing effect of gonadal estrogens. Common Turner skeletal features such as short metacarpals, cubitus valgus, and various craniofacial and cervical skeletal stigmata are largely caused by a compressive effect of distended lymphatics and lymphedema on the developing skeletal tissues.
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J Clin Endocrinol Metab
October 2024
Department of Endocrinology, Key Laboratory of Endocrinology of National Health Commission, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100730, China.
Context: Turner syndrome (TS) is characterized by a partial or complete absence of the second X chromosome in female. Here, patients with Xp deletion involving SHOX haploinsufficiency caused by unbalanced X-autosome translocations were discussed and considered as TS variants.
Objective: This work aimed to expand the current knowledge of TS and unbalanced X-autosome translocations and to suggest the definition, clinical characteristics, diagnosis workflow and growth hormone (GH) treatment strategy of TS and its variants.
Cytogenet Genome Res
December 2024
Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.
Eur J Hum Genet
June 2024
Shriners Hospital for Children, Montreal, QC, Canada.
Haploinsufficiency of the short stature homeobox-containing (SHOX) gene leads to a phenotypic spectrum ranging from Leri-Weill dyschondrosteosis (LWD) to SHOX-deficient short stature. SHOX nullizygosity leads to Langer mesomelic dysplasia. Pathogenic variants can include whole or partial gene deletions or duplications, point mutations within the coding sequence, and deletions of upstream and downstream regulatory elements.
View Article and Find Full Text PDFAndes Pediatr
April 2024
Instituto de Investigaciones Materno Infantil, Hospital Clínico San Borja Arriarán, Santiago, Chile.
Unlabelled: Growth hormone (GH) is effective in improving height in several conditions.
Objective: To describe the evolution of a group of children who received GH in a tertiary center between 2012-2022.
Patients And Method: Descriptive, retrospective study.
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