hydroxyproline has been researched along with Deafness in 9 studies
Hydroxyproline: A hydroxylated form of the imino acid proline. A deficiency in ASCORBIC ACID can result in impaired hydroxyproline formation.
hydroxyproline : A proline derivative that is proline substituted by at least one hydroxy group.
Deafness: A general term for the complete loss of the ability to hear from both ears.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Cleft palate (28%), micrognathia (17%) and sensorineural hearing loss (9%) are also liable to occur in affected individuals." | 1.25 | Stickler's syndrome (hereditary progressive arthro-ophthalmopathy). ( Polomeno, RC; Popkin, JS, 1974) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| PERKOFF, GT | 1 |
| Enderle, A | 1 |
| von Gumppenberg, S | 1 |
| Rashid, M | 1 |
| Khairi, A | 1 |
| Johnston, C | 1 |
| Popkin, JS | 1 |
| Polomeno, RC | 1 |
| Blehová, B | 1 |
| Păzoutová, N | 1 |
| Hyánek, J | 1 |
| Jirásek, J | 1 |
| Woody, NC | 1 |
| Snyder, CH | 1 |
| Harris, JA | 1 |
| Rosenberg, LE | 1 |
| Durant, JL | 1 |
| Elsas, LJ | 1 |
| Fraser, GR | 1 |
| Friedmann, AI | 1 |
| Patton, VM | 1 |
| Wade, DN | 1 |
| Woolf, LI | 1 |
| Minder, FC | 1 |
| Dubach, UC | 1 |
| Antener, I | 1 |
2 reviews available for hydroxyproline and Deafness
| Article | Year |
|---|---|
FAMILIAL ASPECTS OF DIFFUSE RENAL DISEASES.
Topics: Amyloidosis; Angiokeratoma; Blood; Congenital Abnormalities; Deafness; Genetics, Medical; Hematuria; | 1964 |
Treatment of Paget's disease of bone (osteitis deformans) with sodium etidronate (EHDP).
Topics: Alkaline Phosphatase; Bone and Bones; Calcitonin; Calcium; Deafness; Etidronic Acid; Fractures, Bone | 1977 |
7 other studies available for hydroxyproline and Deafness
| Article | Year |
|---|---|
[Osteitis deformans (Paget)--or a tarda-type of a hereditary hyperphosphatasia (author's transl)].
Topics: Adult; Alkaline Phosphatase; Bone Transplantation; Calcitonin; Deafness; Diagnosis, Differential; Di | 1979 |
Stickler's syndrome (hereditary progressive arthro-ophthalmopathy).
Topics: Adolescent; Child; Child, Preschool; Cleft Palate; Deafness; Genes, Dominant; Genetic Counseling; Hi | 1974 |
Iminoglycinuria in a child in Czechoslovakia.
Topics: Amino Acid Metabolism, Inborn Errors; Cerebrospinal Fluid Proteins; Deafness; Female; Glycine; Human | 1973 |
Hyperprolinemia: clinical and biochemical family study.
Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Brain; Bronchopneumonia; Central Nervous System | 1969 |
Familial iminoglycinuria. An inborn error of renal tubular transport.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Genotype; Glycine; Het | 1968 |
Iminoglycinuria--a "harmless" inborn error of metabolism?
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Blindness; Consanguinity; Deafness; G | 1968 |
[Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Deafness; Dw | 1965 |