Rare Congenital Syndrome Associated With Profound Hearing Loss
- 1 April 1979
- journal article
- case report
- Published by American Medical Association (AMA) in JAMA Otolaryngology–Head & Neck Surgery
- Vol. 105 (4) , 222-224
- https://doi.org/10.1001/archotol.1979.00790160056015
Abstract
Research from JAMA Otolaryngology–Head & Neck Surgery — Rare Congenital Syndrome Associated With Profound Hearing LossKeywords
This publication has 3 references indexed in Scilit:
- A syndrome of congenital aplasia of the alae nasi, deafness, hypothyroidism, dwarfism, absent permanent teeth, and malabsorptionThe Journal of Pediatrics, 1971
- Familial Syndrome Combining Deaf-Mutism, Stippled Epiphyses, Goiter and Abnormally High PBI: Possible Target Organ Refractoriness to Thyroid Hormone12Journal of Clinical Endocrinology & Metabolism, 1967
- Oculodentodigital dysplasiaThe Journal of Pediatrics, 1963