20501 to 20600 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

• Macrophage Infiltration of Dermis
• Chronic Deep Dermatophytosis
• Dermatophytic Invasion of Bone
• Dermatophytic Lymphadenitis
• Tinea Capitis Severe or Recurrent
• Dermatophytic Invasion of Gastrointestinal Tract
• Caused by Mutation in the CD96 Gene
• Femur Bent to Lateral Convex Position
• Knobby, Rounded Ends of Femur and Radius
• Short Legs Especially in the Proximal Part
• Birth Length <38 cm
• Mutation in the RECQL3 Gene
• Acute Apnea
• 'Intestinal Pseudotuberculosis'
• Sensitivity to Hypercapnia and Hypoxemia Decreased
• Abnormal Respiration due to Defect in Autonomic Function
• Periods of Apnea
• Distal Muscular Atrophy due to Peripheral Neuropathy
• Poor Outcome
• Cardiac Failure at Birth
• Malposition of the Great Arteries
• Single Ventricle with Right Ventricular Morphology
• Univentricular Atrial-Ventricular Connection
• Complex Heart Malformation
• Trilobulated Lungs Bilaterally (2 Morphologic Right Lungs)
• Expiratory Apnea with Cyanosis
• Caused by Mutation in the Argininosuccinate Lyase Gene
• Plasma Hepcidin Inappropriately Normal or Increased
• Caused by Mutation in the Tyrosinase Gene
• Tyrosinase Activity Absent
• Albinotic Optic Disc
• Mutation in the ELANE Gene
• Promyelocytes Increased
• Up to 3-fold Increase in Blood Monocytes
• Absolute Neutrophil Count Decreased (0.0-0.2*10^9/l)
• Recurrent Severe Infections
• Autosomal Recessive Inheritance Reported in One Case
• Muscle Strength and Bulk is Preserved
• Hemolysis May Be Exercise-Induced
• Episodes of Fatigue or Weakness
• Splenectomy Increases Thrombotic Risk in These Patients
• Mutation in the PIEZO1 Ion Channel Gene
• Susceptibility to Thrombosis
• Perinatal Pleural Effusion
• Increased Hemolysis by Shear Stress
• Increased Red Blood Cell Membrane Permeability to Univalent Cations
• Ektacytometric Osmotic Gradient Curve Shifted to the Left
• Eccentrocytes
• Hepatosiderosis
• Perinatal Ascites
• Contiguous Gene Syndrome Involving Mutation of Genes on 7q11.2
• Considered a Benign Disorder
• Mean Corpuscular Volume May Mildly Increased or Normal
• Cobalamin Decreased
• Death in Utero or in the Perinatal Period
• Mutation in the Integrin Alpha 8 Gene
• Ears Deficient in Cartilage
• Large Low Set Ears
• Ureteral Aplasia
• Cystic Areas of Bone Rarefaction - Especially Phalanges
• Bleeding after Surgery Increased
• Platelets Have Decreased Expression of Glycoprotein Ib Alpha
• Megakaryocytes Are Abnormally Stretched Along Bone Marrow Sinuses
• Megakaryocytes with Hypolobulated Nuclei or Separated Nuclei
• Megakaryocytes Have Dysplastic Features
• Abnormal Megakaryocytes Increased (Bone Marrow)
• Variable Reductions in Platelet Aggregation
• α-Granules in Platelets Decreased or Absent
• Gray Platelets
• Moderate to Severe Bleeding Tendency
• Some Patients Show No Bleeding Abnormalities
• Caused by Mutation in the Integrin Beta 3 Gene
• Caused by Mutation in the Integrin Alpha 2B Gene
• Variable Platelet Functional Defects
• Bleeding Tendency Mild Mucocutaneous
• Small Pelvis Necessitates Caesarean Section
• Duplication of 59 kb on Chromosome 2q35
• Cutaneous Syndactyly of Toes (Usually 2nd and 3rd Toes)
• No Bony Syndactyly
• Cutaneous Syndactyly of Fingers - Usually 3rd and 4th Fingers
• Acrocephalosyndactyly
• Associated with Autoantibodies to GLRA1
• Approximately 10% of Cases Are Paraneoplastic
• Onset in Adolescence or Young Adulthood Has Been Reported
• Onset Usually in 3rd or 4th Decade of Life
• Mutation in the Myotilin Gene
• Possibly Respiratory Difficulties due to Muscle Weakness
• Streaming of the Z Disk Seen on Electron Microscopy
• Muscle Fibers Contain Internal Nuclei
• Spheroid Bodies Are Composed of Fine Filamentous Myofibrillar Material
• Muscle Biopsy Shows 'Spheroid Bodies' in Type 1 Muscle Fibers
• EMG Shows Myopathic Features
• Muscle Pain and Cramping on Exertion
• Downturned Oral Commissures
• Unusual Eyebrow Pattern
• Mildly Dysmorphic Facies
• Weight <25th Percentile
• Hoarse Voice due to Laryngeal Palsy
• Laryngeal Palsy
• Respiratory Insufficiency in Infancy