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16 Possible Causes for Coarse Facial Features, Hoarseness, Mean Corpuscular Volume Increased

  • Chronic Alcoholism

    Serum electrolytes, mean corpuscular volume (MCV) and serum uric acid levels are also indicative of ALD in combination with results from other tests.[] There is increased serum activity of gamma glutamyl transpeptidase (GGTP) in chronic alcohol users.[]

  • Congenital Hypothyroidism

    The child may also have: Poor feeding, choking episodes Constipation Dry, brittle hair Hoarse cry Jaundice (skin and whites of the eyes look yellow) Lack of muscle tone ([] The symptoms of congenital hypothyroidism may include the following: Puffy face Coarse facial features Dull look Thick protruding tongue Poor feeding Choking episodes Constipation[] Two infants who have coarse facial features and growth and developmental delay. Pediatrics in Review, 24 , 16–21.[]

  • Juvenile Myxedema

    Symptoms of this rare but potentially deadly complication include enlarged tongue, swollen facial features, hoarseness, and physical and mental sluggishness.[] […] consumption of goitrogens (e.g. cassava) Symptoms of hypothyroidism Tiredness, weakness Dry skin Feeling cold Hair loss Constipation Weight gain with poor appetite Dyspnea Hoarse[] We will find pressure symptoms such as hoarseness, dysphagia, aphonia, tightness in the throat, a feeling of pressure over the neck, stridor, coughing and hoarseness.[]

  • Sporadic Goitrous Cretinism

    Cretinism  Fetal or infantile hypothyroidism  Endemic and sporadic  Sporadic –agenesis ,dyshormonogenesis  Hoarse cry, macroglossia, umbilical hernia  Immediate diagnosis[] The cretin is generally deaf and dumb, or only able to give a hoarse cry. He is indifferent to heat and cold, and even to the most revolting odors.[] Constipation is a normal rule. j) Speech is slow and sluggish, voice is hoarse.[]

  • Glutamate Formiminotransferase Deficiency

    Peripheral neuropathy, myopathy, hoarseness, and hearing loss Cerebellar ataxia infantile with progressive external ophthalmoplegia 5-Oxoprolinase deficiency ABO BLOOD GROUP[] Clinical signs of the severe form include hernias, facial dysmorphism (macroglossia, constantly opened mouth, coarse features), hepatosplenomegaly, limited joint motion, carpal[] […] recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia Autosomal recessive Charcot-Marie-Tooth disease type 2B1 Autosomal recessive Charcot-Marie-Tooth disease with hoarseness[]

  • Pelviscapular Dysplasia

    […] transient compartment-like syndrome 4 Cases 139426 Perioral myoclonia with absences 10 Cases 563 Peripartum cardiomyopathy 30.0 BP 397744 Peripheral neuropathy- myopathy-hoarseness-hearing[] facial features Gait ataxia Absent speech Patent ductus arteriosus Congestive heart failure Intellectual disability, mild Infantile onset Spasticity Forearm reduction defects[] mean corpuscular volume, Attention deficit hyperactivity disorder, Metopic synostosis, Heart murmur, Ventricular septal defect, Attention deficit hyperactivity disorder,[]

  • Schinzel-Giedion Syndrome

    Other findings include cutaneous ezema, high-pitched or hoarse voice, hypospadias and cryptorchidism.[] This syndrome is characterized by coarse facial features such as midfacial retraction, bulging forehead, short nose with anteverted nostrils, low-set malformed ears, protruding[] […] muscle fatiguability Abnormal electroretinogram Decreased mean corpuscular volume Myoglobinuria Progressive encephalopathy Facial hypotonia Rhabdomyolysis Acute kidney injury[]

  • Smith Lemli Opitz Syndrome

    The children did not have a triangular face, hoarse voice, bulbous nose or abnormal ears; eczema was present in one of the children.[] Face Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations[] In addition, fetal red cell mean corpuscular volume rose, which further indicated that the exogenous cholesterol was incorporated into the fetal erythrocytes.[]

  • Dysmyelination with Jaundice

    A: Compression or destruction of nerve (e.g. recurrent laryngeal nerve by lung or thyroid cancer causes hoarseness) Q: What causes the paraneoplastic effect gout?[] General nonneurologic manifestations of neurometabolic disorders include skeletal abnormalities and coarse facial features (e.g., with muco-polysaccharidoses), macular or[] Abnormal laboratory studies included a haematocrit of 0.67, a haemoglobin of 2.25 g/l, and a mean corpuscular volume of 79.3 fL.[]

  • Thyro-Cerebro-Renal Syndrome

    This is a self-limiting, typically non-life-threatening disorder that mostly affects middle-aged women and is associated with thyroid pain, difficulty swallowing, hoarseness[] Pale, yellow skin; loss of the outer edge of the eyebrows; thin and brittle hair; coarse facial features; brittle nails; firm swelling of the arms and legs; and mental slowing[] The majority of patients have increased mean corpuscular volume, elevated erythrocyte adenosine deaminase activity, and persistence of hemoglobin F.[]

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