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Specialty. Ophthalmology. Retinopathy of prematurity ( ROP ), also called retrolental fibroplasia ( RLF) and Terry syndrome, is a disease of the eye affecting prematurely born babies generally having received neonatal intensive care, in which oxygen therapy is used because of the premature development of their lungs. [ 2]
Ocular hypertension. Ocular hypertension is the presence of elevated fluid pressure inside the eye ( intraocular pressure ), usually with no optic nerve damage or visual field loss. [ 1][ 2] For most individuals, the normal range of intraocular pressure is between 10 mmHg and 21 mmHg. [ 3][ 4] Elevated intraocular pressure is an important risk ...
Idiopathic, brain tumor. In medicine, precocious puberty is puberty occurring at an unusually early age. In most cases, the process is normal in every aspect except the unusually early age and simply represents a variation of normal development. There is early development of secondary sex characters and gametogenesis also starts earlier.
Noonan syndrome ( NS) is a genetic disorder that may present with mildly unusual facial features, short height, congenital heart disease, bleeding problems, and skeletal malformations. [ 1] Facial features include widely spaced eyes, light-colored eyes, low-set ears, a short neck, and a small lower jaw. [ 1]
Hypertensive disease of pregnancy. Hypertensive disease of pregnancy, also known as maternal hypertensive disorder, is a group of high blood pressure disorders that include preeclampsia, preeclampsia superimposed on chronic hypertension, gestational hypertension, and chronic hypertension. [3]
Polycoria. Polycoria is a pathological condition of the eye characterized by more than one pupillary opening in the iris. [1] It may be congenital or result from a disease affecting the iris. [1] It results in decreased function of the iris and pupil, affecting the physical eye and visualization.
11β-OH CAH is autosomal recessive. The enzyme which mediates 11β-hydroxylase activity is now known as P450c11β since it is one of the cytochrome P450 oxidase enzymes located in the inner mitochondrial membrane of cells of the adrenal cortex. It is coded by a gene at 8q21-22. Like the other forms of CAH, a number of different defective ...
1 in 40,000 newborns [1] Leber congenital amaurosis ( LCA) is a rare inherited eye disease that appears at birth or in the first few months of life. [2] It affects about 1 in 40,000 newborns. [1] LCA was first described by Theodor Leber in the 19th century. [3] [4] It should not be confused with Leber's hereditary optic neuropathy, which is a ...