Sitemap | Symptoma 25501 to 25600 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Lack of Skein-Like Inclusions Intraneuronal Inclusions Brisk Reflexes Lack of Upper Motor Neuron Signs Caused by Mutation in the Acylglycerol Kinase Gene Feeding Difficulties Ameliorate with Age Phenotype and Severity Variable Rib Fusion Ectopic Dorsal Pontine Transverse Bundle of Fibers Forms the 'Cap' Hypoplastic or Absent Middle Cerebellar Peduncles Absence of the Inferior Olives Flattening of the Ventral Pons (MRI) Cranial Nerve Dysfunction Ankle Clonus No Motor Skills Acquired Head Titubations Recurrent Cellulitis Relative Brachydactyly Fleshy and Overfolded Helices Low-Normal Height Pectus Excavatum Below Caused by Mutation in the Coiled Coil Domain Containing Protein 103 Recurrent Cough Variable Inner and Outer Dynein Arm Defects Loss of Ciliary Beat Coordination Poor Visual Attention Loss of Motor Neurons in the Spinal Cord Loss of Cerebellar Granular Cells Lack of Motor Milestones Profound Global Developmental Delay Posterior Wall Thickness Increased Interventricular Septum Thickness Increased Periodic Pre- and Postovulation Fever Luteal Phase-Dependent Periodic Fever High Fever Recurrent with Each Menstrual Cycle Affected Males with Serotonin-Related Disorders like Migraine - Headaches - Diabetes Symptoms Relieved by Serotonin Antagonist Symptoms Relieved by Progesterone Antagonist Symptoms Relieved by Ovarian Suppression Mutation in the HTR1A Gene IL-6 Continuously Increased TNF Continuously Elevated Fetal Loss after 6-7 Weeks of Gestation Recurrent Spontaneous Abortion Myalgia with Febrile Episodes Lower Extremity Weakness with Febrile Episodes Ataxia with Febrile Episodes Tremor with Febrile Episodes Diabetes - in Affected Males Mild Hypercortisolism Mutation in the CEP135 Gene Myocytes with Nuclei of Globular Morphology Diffuse Mild Endocardial Fibrosis Focal Mild Interstitial Fibrosis Mutation in the Phospholipase C Beta 4 Gene Mutation in the GUCY2C Gene Prolonged Diarrhea in Infancy Microcolon on Contrast Enema Inspissated Meconium in Distal Ileum Failure to Pass Meconium after Birth Premature Pubarche Elevated Androgen Metabolite Excretion Level Cortisol Excretion Rate Increased High Absolute Level of Cortisone Metabolites Cortisol Metabolites Decreased to Normal Cortols : Cortolone Ratio Low This Patient Died at Age 2 Years Activity of Complexes II and III Decreased Decreased Coenzyme Q10 Poor Responsiveness Hypertonia - Peripheral Dystonia Mutation in the DST Gene Episodic Sweating Episodic Erythematous Blotching Hip Extension Restricted Few Fungiform Papillae on the Tongue Persistently Open Mouth Small Chin Paucity of Facial Expression Pain Response Decreased Lack of Neurologic Development This Patient Died at Age 8 Months Bilateral Signals in the Basal Ganglia Early-Onset Deafness Respiratory Complex I+III and II+III Activity Decreased Possibly Response to Oral Coenzyme Q Possibly Death in Childhood due to End Stage Renal Disease Mutation in the Homolog of the S Cerevisiae COQ6 Gene Diffuse Mesangial Sclerosis Most Patients Die in First Years of Life Mutation in the Isoprenoid Synthase Domain Containing Protein Gene Limb Deformations Arrested Retinal Development Disruption of the Basal Lamina (Skeletal Muscle Biopsy) Brain Vascular Anomalies Subcortical Heterotopia Acentric or Irregular Corneal Video Keratography Shapes Stromal Scar Tissue Fragmentation of Bowman Membrane Subepithelial Fibrosis
