Informaţii despre

Nume Ptosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Ptosis of eyelid
Clasificare anatomică Malacards Boli ale ochiului
Boli din aceeaşi familie Congenital Ptosis; Ptosis, Hereditary Congenital 1; Ptosis, Hereditary Congenital 2

Vezi şi

Boli A-Z 18p Deletion Syndrome Adenocarcinoma Adenoma Aging Albright's Hereditary Osteodystrophy Alopecia Alopecia Areata Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Amblyopia Amenorrhea Aneurysm Anhidrosis Aniridia 1 Anisometropia Ankyloglossia Anorexia Nervosa 1 Anterior Uveitis Apraxia Apraxia of Eyelid Opening Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Autonomic Dysfunction Autosomal Dominant Optic Atrophy Plus Syndrome Axenfeld-Rieger Syndrome Baraitser-Winter Syndrome Baraitser-Winter Syndrome 1 Bethlem Myopathy 1 Bleeding Disorder, Platelet-Type, 11 Blepharochalasis Blepharophimosis Blepharophimosis, Ptosis, and Epicanthus Inversus Blepharospasm Blood Group--Ahonen Brachial Plexus Neuritis Brachydactyly Breast Cancer Breast Disease Breast Reconstruction Carotid Artery Dissection Cataract Cat-Scratch Disease Cellulitis Central Core Myopathy Cerebellar Hypoplasia Cervicitis Charcot-Marie-Tooth Disease, Dominant Intermediate B Chromosome 3q Deletion Chronic Inflammatory Demyelinating Polyneuropathy Chronic Inflammatory Demyelinating Polyradiculoneuropathy Chronic Progressive External Ophthalmoplegia Cluster Headache Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Fiber-Type Disproportion Congenital Hypothyroidism Congenital Myasthenic Syndrome Associated with Acetylcholine Receptor Deficiency Congenital Oculomotor Nerve Palsy Congenital Ptosis Conjunctivitis Conversion Disorder Corneal Disease Cranial Nerve Disease Cranial Nerve Palsy Cutaneous Leishmaniasis Cysticercosis Cytophagic Histiocytic Panniculitis Dacryoadenitis Demyelinating Polyneuropathy Diabetes Mellitus Distal Arthrogryposis Distichiasis Dry Eye Syndrome Duane Retraction Syndrome Dwarfism Dysostosis Dysphagia Ectodermal Dysplasia Ectropion Elephantiasis Enophthalmos Entropion Epicanthus Epidermolysis Bullosa Epidermolysis Bullosa Simplex Epilepsy Esotropia Exophthalmos Exotropia Exposure Keratitis Facial Nerve Disease Facial Paralysis Fanconi Anemia, Complementation Group E Fibrosis of Extraocular Muscles, Congenital, 2 Gastric Adenocarcinoma Giant Papillary Conjunctivitis Gigantomastia Gliomatosis Cerebri Goldberg-Shprintzen Syndrome Guillain-Barre Syndrome Gynecomastia Hansen's Disease Headache Head Injury Hemifacial Microsomia Hemifacial Spasm Hepatocellular Carcinoma Hidrocystoma Hydronephrosis Hypertelorism Hypertropia Hypogonadism Hypomelanotic Disorder Hypotonia Hypotropia Inclusion Body Myositis Infant Gynecomastia Internuclear Ophthalmoplegia Iridocyclitis Iritis Isolated Duane Retraction Syndrome Jorgenson Lenz Syndrome Juvenile Myasthenia Gravis Kallmann Syndrome Kaufman Oculocerebrofacial Syndrome Kearns-Sayre Syndrome Keratoconus Keratopathy Lagophthalmos Lambert-Eaton Myasthenic Syndrome Learning Disability Leber Congenital Amaurosis Leigh Syndrome Leishmaniasis Leukemia Limb-Girdle Muscular Dystrophy Linear Scleroderma Locked-in Syndrome Lung Cancer Lyme Disease Lymphedema Lymphoblastic Leukemia Malignant Hyperthermia Malignant Hyperthermia Susceptibility Marcus Gunn Phenomenon Megacolon Microcephaly Moebius Syndrome Multiple Pterygium Syndrome, Escobar Variant Multisystemic Smooth Muscle Dysfunction Syndrome Muscular Dystrophy Myasthenia Gravis Myasthenia Gravis Congenital Myasthenic Syndrome, Congenital, 4c, Associated with Acetylcholine Receptor Deficiency Myeloma, Multiple Myopathy Myopathy, Centronuclear, 1 Myopia Myositis Myotonia Myotonia Congenita, Autosomal Dominant Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuromuscular Disease Neuromyelitis Optica Neuropathy Ocular Motility Disease Oculomotor Nerve Paralysis Oculopharyngeal Muscular Dystrophy Ohdo Syndrome Orbital Cancer Orbital Tenonitis Ovarian Cyst Panniculitis Papillary Conjunctivitis Paralytic Squint Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Phimosis Pituitary Adenoma Pituitary Apoplexy Plasmacytoma Plexiform Neurofibroma Polydactyly Polyneuropathy Polyradiculoneuropathy Precocious Puberty Premature Menopause Premature Ovarian Failure 1 Primary Hypertrophic Osteoarthropathy Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Propionic Acidemia Ptosis, Hereditary Congenital 2 Purpura Purpura Simplex Radiculopathy Radioulnar Synostosis Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation Refractive Error Rosai-Dorfman Disease Scoliosis Seizures, Benign Familial Neonatal, 1 Sensorineural Hearing Loss Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Spastic Diplegia Spasticity Stormorken Syndrome Strabismus Synostosis Takayasu Arteritis Tay-Sachs Disease Telecanthus Tetanus Three M Syndrome 1 Thrombocytosis Thrombosis Tolosa-Hunt Syndrome Tremor Tukel Syndrome Uremia Uveitis Vernal Conjunctivitis Wisconsin Syndrome