Sitemap | Symptoma 21801 to 21900 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Number of Naive T-Cells Reduced Marked Reduction in CD4+ / CD8+ Ratio Increase in B Cells Increase in CD8+ T Cells Reduced Number of CT4+ T Cells Frequent Infections in Childhood Early-Onset Severe Obesity Sympathetic System Dysfunction Sex Hormone Binding Globulin Levels Low Hypothalamic Hypogonadism Leptin Levels High Leptin Levels Low Variable Ictal Semiology Ventricular Septal Hypertrophy Caused by Mutation in the Keratin 74 Gene Respiratory Insufficiency Requiring Mechanical Ventilation Sural Nerve Biopsy Shows Lack of Myelinated Fibers Intractable Seizures Increased Susceptibility to Malignant Hyperthermia Caused by Mutation in the Phosphoglucomutase-1 Gene Decreased Phosphoglucomutase 1 Activity (<10% of Normal Value) Glycogen Accumulation Seen on Biopsy Phenotype Identical to that of LCCS3 Mutation in the Slow Type Myosin Binding Protein C Gene Muscle Atrophy, Primarily in the Legs Mutation in the PEX10 Gene Plasma Pipecolic Acid Increased Plasma Phytanic Acid Increased Plasma Pristanic Acid Increased Branched-Chain Fatty Acids Increased Distal Muscle Atrophy Bile Acid Intermediates DHCA and THCA Increased Pristanic Acid Increased Very Long-Chain Fatty Acids Normal or Increased Normal Anterior Pituitary Function Gonadotropin Decreased Mutation in the Gonadotropic Releasing Hormone 1 Gene Few to No Follicles on Ultrasonography Variable Expressivity within a Family Mutation in the KISS1 Receptor Gene Near Normal Pubic Hair Number of Follicles Seen on Ultrasound Reduced Small Ovaries Low Testosterone in Males Partial or Complete Gonadotropin Deficiency Eunuchoid Appearance of Males Flunarizine Treatment May Be Beneficial Levels of Certain Coagulation Factors Decreased Some Patients May Not Have Recurrent Infections Highly Variable Clinical and Immunologic Phenotype Fibrosing Pneumonitis Numbers of T Regulatory Cells Decreased Defective T Cell Proliferative Responses Villous Blunting Progressive Postnatal Microcephaly Atrophy of the Pons Global Developmental Delay of Variable Severity PTH Mildly Increased Urinary Excretion of Pyridinoline Normal Retrogenia in Infancy Redundant Umbilical Skin Congenital or Perinatal Onset Neuronal Loss in the Striatum, Cerebral Cortex and Cerebellum High Voltage Spikes Over the Temporal and Central Regions Caused by Somatic Mutations Somatic Mutation in the KRAS Gene Alpha/Beta+ CD4-/CD8- T Cells Normal or Mildly Increased B-Cell Lymphocytosis Risk of Hematologic Malignancy Increased Dull-Appearing Central Foveal Reflex Tigroid-Appearing Fundus Intracranial Aneurysms Aberrant Gamma Interferon-Mediated Inflammation Immunoglobulins Progressively Decreased Decreased Memory B Cells Progressive Progressive Lymphopenia Disseminated Infection with Dimorphic Fungi Recurrent Infections - Bacterial Viral Fungal Myobacterial Chronic Recurrent Candidiasis Villous Atrophy Puberty Delayed Pale Hair Lack of Dense Granules in Platelets Bleeding Tendency due to Platelet Defect Variable Features and Severity Mutation in the CFC1 Gene Mutation in the Transcription Factor SP7 Gene Some Patients May Benefit from Coenzyme Q10 Treatment Coenzyme Q10 Levels in Muscle Decreased Mild Lower Motor Neuron Involvement (EMG) Onset of Symptoms in First Decade of Life Mutation in the KCNJ5 Gene Severe Hypertension Hypotonic Urine Histologically Normal Adrenal Gland Atrophic Zona Glomerulosa of Adrenal Gland Hyperplasia of Zona Glomerulosa of Adrenal Gland Hyperplasia of Zona Fasciculata of Adrenal Gland Aldosterone Secretion Elevated Hypokalemia Related Muscle Weakness
