Create issue ticket

93 Possible Causes for Hyperhidrosis, Muscle Mass Decreased, Xeroderma

  • Chronic Alcoholism

    Low body temperature Muscle weakness and atrophy ( loss of tissue mass ) Problems with walk (gait) and coordination The person may appear poorly nourished.[medlineplus.gov] Examination of the nervous/muscular system may show damage to many nerve systems: Abnormal eye movement Decreased or abnormal reflexes Fast pulse (heart rate) Low blood pressure[medlineplus.gov]

  • Diabetes Mellitus

    Glucose levels also take longer to return to normal, in part because of increased accumulation of visceral and abdominal fat and decreased muscle mass.[merck.com] muscle mass.[web.archive.org] […] younger adults, especially after high carbohydrate loads, and take longer to return to normal, in part because of increased accumulation of visceral and abdominal fat and decreased[web.archive.org]

  • Menopause

    Also known as “sleep hyperhidrosis”, night sweats aren't actually a sleep disorder, but a common perspiration disorder that occurs during sleep in menopausal women.[34-menopause-symptoms.com] Due to a decrease in muscle mass and slowing of your metabolism, it’s more important than ever to limit processed foods and focus on eating a clean diet.[draxe.com] Metabolism through menopause may decrease by 10 to 15 per cent; this is more significant if muscle mass going into menopause is low.[thisnzlife.co.nz]

  • Exfoliative Ichthyosis

    […] verrucous papilloma vulvar squamous papilloma X-linked ichthyosis xeroderma of eyelid Zunich Neuroectodermal Syndrome[rgd.mcw.edu] We present a 25-year-old man from Iran with consanguineous parents, who presented with congenital erythroderma, hyperhidrosis and diffuse hyperkeratosis with coarse palmoplantar[ncbi.nlm.nih.gov] The situation is similar to that observed in patients following burns (negative nitrogen balance characterized by edema, hypoalbuminemia, loss of muscle mass).[emedicine.medscape.com]

  • Camurati-Engelmann Syndrome

    Rare signs include sensory loss, slurred speech, dysphagia, cerebellar ataxia, anorexia, decreased subcutaneous tissue, hyperhidrosis of the extremities, delayed dentition[orpha.net] […] syndrome Autosomal dominant intermediate Charcot-Marie-Tooth Genitopatellar syndrome Keratoderma palmoplantar deafness Congenital primary aphakia Russell-Silver syndrome Xeroderma[checkrare.com] Hepatosplenomegaly, Raynaud's phenomenon, hyperhidrosis of the feet and hands, and delayed dentition and puberty have been reported ocassionally. 15 Anemia, leukopenia, increased[elsevier.es]

  • CAMFAK Syndrome

    He is also the Editor of Molecular Mechanisms of Fanconi Anaemia, Molecular Mechanisms of Xeroderma Pigmentosum, Molecular Mechanisms of Ataxia Telangiectasia and Molecular[books.google.com] […] hypoplasia Macrotia Weak cry Limb muscle weakness Severe postnatal growth retardation Severe intrauterine growth retardation Tics Hyporeflexia Constipation Respiratory failure Hyperhidrosis[mendelian.co] […] a nucleotide excision repair (NER) defect: xeroderma pigmentosum (XP), Cockayne syndrome (CS), and the photosensitive form of trichothiodystrophy (TTD).[ommbid.mhmedical.com]

  • Spastic Ataxia with Congenital Miosis

    The visible scale differentiates these disorders from xeroderma in which the skin is dry but does not visibly desquamate.[pediatrics.aappublications.org] Depressivity Upper limb hypertonia Retinopathy Adult onset Oromandibular dystonia Pain Sensory neuropathy Peripheral axonal neuropathy Distal amyotrophy Spastic paraplegia Hyperhidrosis[mendelian.co] FLACCID PARAPLEGIA  decreased tone and contractility of muscles along with weakness.  it occurs in lower motor neuron diseases  due to loss of stimulatory innervation to[slideshare.net]

  • Myelocerebellar Disorder

    Sparse scalp hair Cerebral calcification Decreased testicular size Abnormality of skin pigmentation Pulmonary fibrosis Nail dystrophy Ranula Muscular hypotonia of the trunk Hyperhidrosis[mendelian.co] 1911000 Tuberous sclerosis -1933000 Von hippel-lindau syndrome -1940700 Wilms tumor 1 -1940800 Denys-drash syndrome nephropathy wilms tumor and genital anomalies -1944000 Xeroderma[julesberman.blogspot.com] 1 Hyperglycinemia, isolated nonketotic type 2 Hyperglycinemia, isolated nonketotic Hyperglycinemia Hypergonadotropic ovarian failure, familial or sporadic Hyperh–Hyperk Hyperhidrosis[sosu.us]

  • Arthrogryposis due to Muscular Dystrophy

    […] pigmentosum, Xeroderma pigmentosum/Cockayne syndrome AR 21 54 ERCC6 * Xeroderma Pigmentosum-Cockayne Syndrome, De Sanctis-Cacchione syndrome AD/AR 87 135 EXOSC3 Pontocerebellar[blueprintgenetics.com] Additional clinical findings were onset in the neonatal period or early infancy, which included generalized muscle weakness, hyperhidrosis, high-arched palate, protruded calcanei[medlink.com] Structural abnormalities of kidneys, ureters, and bladder Decreased muscle mass, soft muscle texture, fibrous bands, abnormal tendon attachments.[boneandspine.com]

  • Congenital Muscular Dystrophy Type Ullrich

    Congenital 2 with or without Brain or Eye Anomalies via MPDZ Gene Sequencing with CNV Detection ( #12013 ) Pediatric Cancer Sequencing Panel with CNV Detection ( #7973 ) Xeroderma[preventiongenetics.com] Additional clinical findings were onset in the neonatal period or early infancy, which included generalized muscle weakness, hyperhidrosis, high-arched palate, protruded calcanei[medlink.com] Open mouth Narrow face Decreased muscle mass Thoracic kyphosis Facial diplegia Nemaline bodies Distal lower limb amyotrophy Myokymia Distal lower limb muscle weakness Hypoplasia[mendelian.co]

Similar symptoms