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crysis crack 1.1.1.5767We report a case of a 50-year-old male with short stature, high-pitched voice, and excessive sweating. He has been diagnosed as a case of frontometaphyseal dysplasia with hypermobility type, due to the identification of novel *COL2A1* gene mutation and a proposed associated phenotype (frontometaphyseal dysplasia with hypermobility type \[FMD-H\]). Short stature and laryngeal symptoms in this syndrome are not a common finding. This case, along with previous reports, may reveal a novel phenotype of FMD-H in addition to the previously reported cases of FMD-H.

An initially diagnosed case of frontometaphyseal dysplasia, a rare skeletal dysplasia, was referred to the department of pediatric otolaryngology because of laryngeal symptoms. Although the patient had some hoarseness, the voice was not high-pitched. The patient was quite tall (172 cm) and overweight (113 kg, BMI 24.8) with a non-smoker history. Physical examination revealed only hoarseness and excessive sweating. Neck muscle and skin were not swollen. An otolaryngologist made a diagnosis of laryngopharyngeal reflux. The main physical findings were as follows: height 172 cm, weight 113 kg, and BMI 24.8, and the physical findings were as follows: short stature with an increase of 4.7 cm in height and a weight increase of 9.6 kg since the last investigation. The laboratory results were all within normal ranges. Whole-body computed tomography revealed thin cortices of the femur and an irregular radiolucent defect in the bone (Fig. [1](#Fig1){ref-type="fig"}a). A bone scan did not show significant uptake (Fig. [1](#Fig1){ref-type="fig"}b). Fig. 1**a 0b46394aab

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