hypoplasia

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Related to Goltz syndrome: incontinentia pigmenti
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Words related to hypoplasia

underdevelopment of an organ because of a decrease in the number of cells

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The patient may have other associated anomalies9 which include cleft lip and/or palate, abnormal ears, hydrocephalus, cranial/spinal malformations, microphthalmus, congenital heart disease, tracheo-esophageal fistula, omphalocele, anorectal malformation, renal malformation (agenesis, polycystic kidneys), duplication of cervix or uterus, vascular anomalies, nail aplasia or dysplasia, digital anomalies, simian creases, Goltz syndrome (focal dermal hypoplasia), trisomy 13, intestinal lymphangiectasia and pyloric atresia.
1,8) Other syndromes associated with ectrodactyly include Carpenter's syndrome, DeLange syndrome, Goltz syndrome, and Miller syndrome.
Researchers funded in part by the National Institutes of Health have identified the gene that accounts for most cases of Goltz syndrome, a rare skin disorder that can also affect bone and eye development.
Otolaryngological manifestation of Gorlin Goltz syndrome.
MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.