Sitemap | Symptoma 27601 to 27700 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Poor Healing with Abnormal Scarring Soft with Easy Bruising Cornea Plana Megalocornea Hypercompliant Tympanic Membranes Inguinal Umbilical or Epigastric Hernia Onset at Age <7 Years Mutation in the Zinc Finger Protein 644 Gene Myopic Conus Tesselated Appearance of Fundus Tigroid Appearance of Fundus Severe High Myopia Catecholamine-Secreting Paraganglioma Thromboxane B2 Decreased Claw-like Appearance of Fingernails Hyponychia Onychauxis - Thickening Both Heterozygous and Homozygous Mutations Have Been Reported Green Color Resolves if Cholestasis Is Treated Green Jaundice Occurs Only in the Context of Liver Failure or Obstructive Cholestasis Green Jaundice Possibly Bilirubin Increased Biliverdin in Bodily Fluids Increased Green Serum Described in Families from Western Japan Patients with Longer Disease Duration Show Motor Neuron Involvement Mean Age at Onset of Cerebellar Ataxia: 52.8 Years Truncal Instability Onset at Ages 12-30 Years (Average: 22 Years) Flat Audiogram High Frequency Tinnitus at Onset Poor or No Response to Glucocorticoid Treatment Mutation in the MYO1E Gene Thickening and Disorganization of the Glomerular Basement Membrane Microvillous Transformation of Podocytes Electron Microscopy Shows Foot Process Effacement Complement Component Deposits Antibody Deposits Death in Utero Malformations of the Mid- and Hindbrain Death in the Fifth or Sixth Decade Onset of Dementia in 4th or 5th Decade Caused by Mutation in the DNA Methyltransferase 1 Gene Ulceration of the Toes Loss of Unmyelinated Fibers Lancinating Pains Hypometabolism of the Frontal Lobe and Thalamic Regions Frontal Lobe Atrophy Decreased Speech Progressive Memory Impairment Onset of Seizures Ranges from 2 to 11 Years Mutation in the LAMC3 Gene Transient Strabismus Occipital Polymicrogyria Occipital Pachygyria Mild Facial Dysmorphism Abnormal Lung Lobation Clinodactyly Rhizomelic Shortening of the Upper Limbs Small Nose Downslanting Palpebral Fissures Short Palpebral Fissures Triangular Face Long Face Narrow Head Temporal Bossing Feet Are Unaffected Torso and Upper Body Remain Normal in Shape and Contour Virtually all Patients with this Condition Are Female Dependent Edema after Excess Fat Has Been Present for Several Years Easy Bruisability of Lower Extremities Tenderness of Lower Extremities Fat Pad between Achilles Tendon and Medial Malleolus Fat Pad Anterior to Malleolus Burning or Tingling of Plantar Surface of Foot Deficiency of Laminin in Basement Membranes Mild Elbow, Hip and Knee Contractures Bilateral Sandal Gap Bilateral Postaxial Polydactyly Shortening or Bowing of Humeri Rhizomelic Limbs Sagittal Suture Synostosis Everted Lower Lip Telecanthus Neonatal Cholestasis End Stage Renal Disease Large Prominent Eyes Tightly Adherent Facial Skin Normal Growth Parameters at Birth Mutation in the AARS2 Gene Histiocytoid Changes Mild Pulmonary Hypoplasia Periodic Stiffness Death before Age 3 Years Prominent Sutures Lateral Deviation of the 5th Toe Adducted Feet Division of the First Metacarpal Fusion of the Capitate and Hamate Bones Longitudinal Splitting of the Proximal Phalanx of Forefinger
