Create issue ticket

349 Possible Causes for Coarse Facial Features, Hearing Problem

  • Mucopolysaccharidosis

    People with MPS IVB can have lots of problems. They can have skeleton, heart, vision and dental problems, hearing loss, growth deficiency and short stature.[] facial features, developmental delay, and an elevated quantitative urine glycosaminoglycan (GAG) level.[] However, they may present with a variety of physical problems. These may include joint stiffness, heart problems, corneal clouding and hearing loss.[]

  • Fabry Disease

    Hearing problems - This may include a gradual loss of hearing or ringing in the ears (tinnitus).[] Often patients have slight builds with characteristic coarse facial features and delayed puberty.[] The patient is 10 years old and presents severe mental handicap, coarse face, hepatosplenomeagly, dysostosis multiplex, joint contractures, obstructive airway disease, mitral[]

  • Mucopolysaccharidosis 2

    Hearing problems. Swollen and stiff joints. Abdominal hernias. Hepatosplenomegaly.[] Other symptoms may include carpal tunnel syndrome, coarse facial features, deafness, hairy body (hypertrichosis), joint stiffness, and a large head (macrocephaly).[] He may be eligible for one-on-one attention in the classroom or help for other issues, like hearing problems. Take care of yourself, too.[]

  • Mucopolysaccharidosis 1

    By the age of three growth usually slows down significantly and intellectual and hearing problems become apparent.[] Further common findings are coarse facial features, carpal tunnel syndrome, umbilical and inguinal hernia, and hepatomegaly.[] The onset of symptoms usually occurs in early childhood, causing problems of otitis media, hearing loss and airway obstruction in the ENT area.[]

  • Mucopolysaccharidosis 6

    In rare cases, hearing loss may be due to a combination of both problems (mixed hearing loss).[] Presentation Patient with coarse facial features, cardiac murmure, gibbus and dental decay.[] Physical Facial features associated with MPS VI include the following: Coarse facial features (Compare the facial features with those of other family members to best appreciate[]

  • Mucopolysaccharidosis 4A

    Nonskeletal symptoms Breathing problems Heart valve problems Muscle weakness Eye problems Hearing loss Dental problems Enlarged liver Enlarged spleen Limited energy Getting[] facial features Coarse facial appearance 0000280 Constricted iliac wings 0003277 Coxa valga 0002673 Disproportionate short-trunk short stature Disproportionate short-trunked[] Signs & Symptoms Individuals with MPS disorders share many similar symptoms such as multiple organ involvement, distinctive “coarsefacial features, and abnormalities of[]

  • Chronic Alcoholism

    What this means is that problem drinkers can completely misinterpret what they’re seeing and hearing.[]

  • Incontinentia Pigmenti Achromians

    Other symptoms develop as the child grows, and may include: Crossed eyes (strabismus) Hearing problems Increased body hair ( hirsutism ) Scoliosis Seizures Streaked, whorled[] Other associated disorders occur inconsistently and include macrocephaly, microcephaly, h6mihypertrophy, kyphoscoliosis, coarse facial features, genital anomalies, inguinal[] Symptoms Crossed eyes (strabismus) Hearing problems Increased body hair ( hirsutism ) Scoliosis Seizures Streaked, whirled or mottled patchs of skin on the arms, legs, and[]

  • Mandibulofacial Dysostosis

    It depends on the problems your child has, or may have in the future. If your baby does have TCS, you’ll want to get her hearing checked.[] We report a female child born at 36 weeks of gestation with multiple abnormalities including dysmorphic and coarse facial features with features of mandibulofacial dysostosis[] This can cause hearing problems if the ear's internal structures are also underdeveloped.[]

  • Mucopolysaccharidosis 1H

    By the age of three growth usually slows down significantly and intellectual and hearing problems become apparent.[] […] hairy skin all over the body, a tuft of hair in the parietal region, coarse facial features and a prominent forehead with a large tongue, hepatosplenomegaly and skeletal[] facial features with low nasal bridge Signs and tests [ edit ] Genetic testing for the alpha-L-iduronidase (IDUA) gene Urine tests for extra mucopolysaccharides X-ray of[]

Further symptoms

Similar symptoms