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124 Possible Causes for Cardiomyopathy, Thick Coarse Hair

  • Hypothyroidism

    Overt hypothyroidism may exacerbate underlying cardiac disease, but cardiomyopathy severe enough to cause heart failure is rare ( Kahaly 2005 ).[] […] and dry hair; coarse, dry, scaly and thick skin; carotenemia, particularly notable on the palms and soles (caused by deposition of carotene in the lipid-rich epidermal layers[] Ladenson PW, Sherman SI, Baughman KL et al.: Reversible alterations in myocardial gene expression in a young man with dilated cardiomyopathy and hypothyroidism.[]

  • Mucopolysaccharidosis 1H

    Corneal opacities, hepatosplenomegaly, cardiomyopathy and upper airway obstruction are present.[] Others: Other features may include short neck, subluxation of vertebral bodies, thick and coarse body hair and thickened skin.[] Glycosaminoglycans Neurological Dementia, sensorineural hearing loss, White matter abnormalities (MRIscan) Non-Neurological Dysmorphisms, corneal clouding, valvular thickening and cardiomyopathy[]

  • Mucopolysaccharidosis 1

    Cardiomyopathy and coronary heart disease. Hepatosplenomegaly.[] Physical Examination Appearance Short stature with disproportionately short trunk ( dwarfism ) Skin Thickened skin Excessive body hair growth HEENT Coarse or rough facial[] Currently, no patient has any clinical evidence of cardiomyopathy.[]

  • Hypertrichotic Osteochondrodysplasia

    Diseases related with Cardiomyopathy and Short phalanx of finger In the following list you will find some of the most common rare diseases related to Cardiomyopathy and Short[] Patients have thick scalp hair, which may extend onto the forehead, and an overall increase in body hair. read more[] The hypertrichosis leads to thick scalp hair, which extends onto the forehead, and a general increase in body hair.[]

  • Costello Syndrome

    Costello syndrome can complicate fatal hypertrophic obstructive cardiomyopathy.[] […] lips Kyphoscoliosis, cervical kyphosis Remarkably pleasant, sociable, humorous and easy-going personality Adolescents/Adults Coarse classic facial features Thicker, often[] […] palmar and plantar creases, loose joints, distinctive coarse facial features, skeletal abnormalities, cardiac abnormalities (cardiovascular malformation (CVM), hypertrophic cardiomyopathy[]

  • Gangliosidosis GM1

    ", keywords "Angiokeratomas, B-galactosidase, Cherry-red spot, Dystonia, Galactosialidosis, Gangliosidosis, GM1, Hypertrophic cardiomyopathy, Morquio B, Vacuolated lymphocytes[] Infants have coarse thick hair, a depressed nasal bridge, gingival hypertrophy, large low-set ears and hair on the forehead.[] […] overgrowth Gum enlargement 0000212 Hepatomegaly Enlarged liver 0002240 Hypertelorism Wide-set eyes Widely spaced eyes [ more ] 0000316 Hypertrichosis 0000998 Hypertrophic cardiomyopathy[]

  • Hoffmann Syndrome

    Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy: A hitherto unrecognized association.[] […] with thick skin, coarse facial features, depressed nasal bridge, hypertelorism, and puffed lips ( Fig. 3 ).[] […] hypothyroid muscular pseudohypertrophy-a rare report of two cases. ( 22934196 ) Shaw C....Shaw P. 2012 5 Kocher-Debre-Semelaigne syndrome with arrhythmogenic right ventricular cardiomyopathy[]

  • Bjornstad Syndrome

    Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy. Human Mutation 32, 1225-1231.[] Lusterless, opaque, scarce blond hair. FIGURE 2 Pili torti. Thick, coarse and brittle hair in the left occipitotemporal region. FIGURE 3 Pili torti.[] Corrado D, Basso C, Thiene G (2009) Arrhythmogenic right ventricular cardiomyopathy: an update. Heart 95:766–773 CrossRef PubMed 8.[]

  • GM2-Gangliosidosis

    Type 3 GM1 gangliosidosis has an age of onset during adulthood and resembles Parkinson disease with symptoms including an unsteady gait and cardiomyopathy.[] Infants have coarse thick hair, a depressed nasal bridge, gingival hypertrophy, large low-set ears and hair on the forehead.[] Cardiomyopathy may occur. Etiology GM1 gangliosidosis is caused by mutations in the GLB1 gene (3p22.3) coding for beta-galactosidase.[]

  • Amaurosis-Hypertrichosis Syndrome

    Food and Drug Administration granted Priority Review to Pfizer for its application to market tafamidis, its treatment for transthyretin amyloid cardiomyopathy (ATTR-CM), a[] […] eyebrow 60 33 hallmark (90%) Very frequent (99-80%) HP:0000574 3 optic atrophy 60 33 hallmark (90%) Very frequent (99-80%) HP:0000648 4 coarse hair 60 33 hallmark (90%) Very[] , dilated, 1Z) TNNI2 (Arthrogryposis multiplex congenita, distal type 2B) TNNI3 (Cardiomyopathy, dilated, 1FF) TNNT1 (Nemaline Myopathy, Amish Type) TNNT2 (Cardiomyopathy,[]

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