Create issue ticket

34 Possible Causes for Male Hypogonadism, Narrow Shoulders, Skeletal Dysplasia

  • Froehlich's Syndrome

    shoulders, and pre-pubertal penis.[] Testosterone modulates serum leptin concentrations in a male patient with hypothalamic hypogonadism. J Endocrinol Invest. 2000;23:246-50.[] Whilst there are discernible changes in the ‘Amarna’ style as Akhenaten’s reign progresses, generally the upper torso is depicted small with a narrow waist and narrow shoulders[]

  • Klinefelter Syndrome

    After puberty, KS boys may have Smaller testes and penis Breast growth Less facial and body hair Reduced muscle tone Narrower shoulders and wider hips Weaker bones Decreased[] Achondroplasia (ACH), an autosomal dominant skeletal dysplasia, occurs in approximately 1:20,000 births.[] Affected males carry an additional X chromosome, which results in male hypogonadism, androgen deficiency, and impaired spermatogenesis.[]

  • Anorchia

    […] and narrow hips.[] dysplasias 4.11 Glucocorticoid-induced osteoporosis Part 5 The adrenal gland and endocrine hypertension 5.1 Adrenal imaging 5.2 Adrenal surgery 5.3 Adrenal incidentaloma[] Subsequent chapters deal with male sexual precocity; "fertile eunuchism" (Leydig cells reduced in number and size with preserved spermatogenesis); male idiopathic hypogonadism[]

  • Acrocapitofemoral Dysplasia

    […] and to a variable degree in the shoulders, knees, and ankles.[] “Acrocapitofemoral Dysplasia: An Autosomal Recessive Skeletal Dysplasia with Cone Shaped Epiphyses in the Hands and Hips.”[] A novel syndrome of mandibular hypoplasia, deafness, and progeroid features associated with lipodystrophy, undescended testes, and male hypogonadism.[]

  • Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome

    […] chest, sloping shoulders, aged appearance of the hands and feet and facial dysmorphism (beaked nose and severe retrognathia).[] dysplasia 215140 Pelger-Huet anomaly 169400 LEPRE1 1p34.2 Osteogenesis imperfecta, type VIII 610915 LHCGR 2p16.3 Leydig cell adenoma, somatic, with precocious puberty 176410[] males.[]

  • Autosomal Dominant Prognathism

    Fig. 2 The patient demonstrates shoulder joint hypermobility, which is a common clinical finding in cleidocranial dysplasia.[] The authors also have had available data from the University of Cape Town Skeletal Dysplasia Registry.[] Hypogonadism in males/hyperandrogenism in females is also reported.[]

  • Aromatase excess syndrome

    His virilization was incomplete with no facial hair at all, narrow shoulders, small testes (12 ml each), and genital status G4 according to Tanner.[] Skeletal findings.[] Letrozole once a week normalizes serum testosterone in obesity-related male hypogonadism. Eur J Endocrinol 2008;158:741-7. 3.[]

  • Crane-Heise Syndrome

    The main clinical signs are hypoplasia or aplasia of the clavicles with narrow, sloping shoulders that can be approximated anteriorly, delayed fusion of cranial sutures with[] The combination of skeletal dysplasia, seizure disorder and Crane-Heise Syndrome require Faith to wear a soft-shelled helmet because she does not have a cranial cap.[] Hypogonadism with Mental Retardation and Skeletal Anomalies Male Pseudohermaphroditism/Mental Retardation Syndrome, Verloes Type Malignant Carcinoid Syndrome Mammary-Digital-Nail[]

  • Skeletal Dysplasia - Intellectual Disability Syndrome

    […] long neck Facies: epicanthic folds antimongoloid eye slant broad nasal root mild hypertelorism everted prominent lower lip Thorax: growth long and narrow prominent manubrium[] Homepage Rare diseases Search Search for a rare disease X-linked skeletal dysplasia-intellectual disability syndrome Disease definition Skeletal dysplasia-intellectual disability[] For example, a male patient with 3-M syndrome will need to be monitored for the development of hypogonadism.[]

  • Primary Hypergonadotropic Hypogonadism-Partial Alopecia Syndrome

    Additional signs are chest disorder (as a narrow “keeled breast”, sloping shoulders) and adipose tissue deficit.[] dysplasia 60 33 frequent (33%) Frequent (79-30%) HP:0002652 27 microcephaly 60 33 frequent (33%) Frequent (79-30%) HP:0000252 28 intellectual disability, mild 60 33 frequent[] Jordan Al-Awadi et al. (1985) reported three siblings (two females and a male) with primary hypogonadism and partial alopecia.[]

Similar symptoms