Pediatric Ophthalmology, Volume 2 |
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Page 872
... Autosomal recessive . Ophthalmic Manifestations Progressive optic atrophy . Nystagmus . OCULAR CHANGES IN PEDIATRIC SYSTEMIC DISORDERS OCULAR MANIFESTATIONS IN CONNECTIVE. Friedreich's Ataxia Hereditary Cerebellar Ataxia : Types of Marie ...
... Autosomal recessive . Ophthalmic Manifestations Progressive optic atrophy . Nystagmus . OCULAR CHANGES IN PEDIATRIC SYSTEMIC DISORDERS OCULAR MANIFESTATIONS IN CONNECTIVE. Friedreich's Ataxia Hereditary Cerebellar Ataxia : Types of Marie ...
Page 1016
... autosomal dom- inant . 2. Congenital ichthyosiform erythro- derma autosomal dominant . - 3. Bullous congenital ichthyosiform erythroderma autosomal dominant . 4. Lamellar ichthyosis autosomal re- cessive . 5. X - linked ichthyosis ...
... autosomal dom- inant . 2. Congenital ichthyosiform erythro- derma autosomal dominant . - 3. Bullous congenital ichthyosiform erythroderma autosomal dominant . 4. Lamellar ichthyosis autosomal re- cessive . 5. X - linked ichthyosis ...
Page 1057
... autosomal recessive type . That is to say , assuming that no new mutations . occur , the inheritance pattern is such that each parent has to contribute a defective mutant gene to the offspring . If only one of the pair of corresponding ...
... autosomal recessive type . That is to say , assuming that no new mutations . occur , the inheritance pattern is such that each parent has to contribute a defective mutant gene to the offspring . If only one of the pair of corresponding ...
Contents
PEDIATRIC NEUROOPHTHALMOLOGY | 767 |
Pupil Abnormalities | 783 |
DISORDERS OF THE LIDS 412 | 793 |
Copyright | |
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Common terms and phrases
abnormalities acid affected Albinism Amer antibodies antigens Arch associated autoimmune autosomal bilateral blindness C. V. Mosby cataracts cause cells cent cerebral child childhood choroid clinical congenital conjunctiva corneal cranial cyst cystinosis defect deficiency degeneration develop diabetes diagnosis disc disorder drome Duke-Elder dystrophy edema enzyme errors of metabolism Fabry's disease familial fibers fixation frequently fundus Gaucher's disease gaze genetic glaucoma glioma hemorrhage hereditary homocystinuria hypoplasia immune Inborn Errors infection intracranial intraocular involvement iris keratitis lens lenses lesions lipid lymphocytes macrophages macular malignant membrane ment muscle neurologic Niemann-Pick disease normal nystagmus occur ocular manifestations Ophthal Ophthalmology optic atrophy optic nerve optic neuritis orbital palsy papilledema pathologic patients pediatric peripheral pigment pigmentary posterior primary protein ptosis pupillary renal response result retinal detachment retinoblastoma serum signs skin strabismus symptoms syndrome Systemic Table therapy tion tissue trauma treatment tumor usually uveitis vascular vision visual acuity vitamin vitreous