2-propanol and Deafness studies

2-propanol and Deafness

2-propanol has been researched along with Deafness in 40 studies

2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.

Deafness: A general term for the complete loss of the ability to hear from both ears.

Research Excerpts

Excerpt	Relevance	Reference
"Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal root and confluent eyebrows, heterochromia iridum, a white forelock and congenital deafness."	3.64	WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION. ( PARTINGTON, MW, 1964)
"Waardenburg-Klein syndrome is an "Oculo-dermato-auditif" dysplasia described in 1947 by Waardenburg and by Klein in 1950."	2.40	[A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC]. ( Babagbeto, M; Bassabi, SK; Doutetien, C; Hounkpe, YY; Latoundji, S; Medji, AP; Oussa, G; Vodouhe, SJ, 1997)
"One child had an iris coloboma."	1.29	Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder? ( Barrow, M; Donnai, D, 1993)
"Eighty-nine children with the Waardenburg syndrome were identified during diagnostic surveys of 3006 deaf children attending 19 special schools in southern Africa."	1.27	The Waardenburg syndrome in deaf children in southern Africa. ( Beighton, P; Sellars, S, 1983)
"In addition to acronymic features of Coloboma, Heart disease, Atresia of the choanae, Retarded growth and development, Genital hypoplasia, and Ear anomalies, other important diagnostic features include facial paralysis and feeding problems suggestive of velopharyngeal incompetency."	1.27	The spectrum of clinical features in CHARGE syndrome. ( Davenport, SL; Hefner, MA; Mitchell, JA, 1986)

Research

Studies (40)

Timeframe	Studies, this research(%)	All Research%
pre-1990	35 (87.50)	18.7374
1990's	4 (10.00)	18.2507
2000's	1 (2.50)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Timeframe

Studies, this research(%)

All Research%

pre-1990

35 (87.50)

18.7374

1990's

4 (10.00)

18.2507

2000's

1 (2.50)

29.6817

2010's

0 (0.00)

24.3611

2020's

0 (0.00)

2.80

Authors

Authors	Studies
Magdesian, KG	1
Williams, DC	1
Aleman, M	1
Lecouteur, RA	1
Madigan, JE	1
BROBECK, VH	1
FLEISCHLI, CA	1
DIGEORGE, AM	1
OLMSTED, RW	1
HARLEY, RD	1
PARTSCH, CJ	1
HOUGHTON, NI	1
COUTEAU-LAGARDE, JM	1
COLLIER, M	1
PARTINGTON, MW	1
NATH, K	1
VIJAY, SD	1
NEMA, HV	1
SHUKLA, BR	1
RUGEL, SJ	1
KEATES, EU	1
PAUFIQUE, L	1
RAVAULT, MP	1
MORGON, A	1
ROBINSON, GC	3
MILLER, JR	1
SOEPARDEN, LI	1
POROT, M	2
FILIU, M	1
Uyama, S	1
Aikawa, K	1
Tomemori, S	1
Feingold, M	1
Robinson, MJ	1
Gellis, SS	1
Sellars, S	1
Beighton, P	1
Donnai, D	1
Barrow, M	1
Bassabi, SK	1
Medji, AP	1
Doutetien, C	1
Oussa, G	1
Hounkpe, YY	1
Vodouhe, SJ	1
Babagbeto, M	1
Latoundji, S	1
Bard, LA	1
Hayasaka, S	1
Noda, S	1
Setogawa, T	1
Kobayashi, A	1
Kishida, K	1
Sakai, T	1
Warburg, M	1
Tommerup, N	1
Vestermark, S	1
Parving, A	1
Weismann, K	1
Russell, B	1
Thomsen, HK	1
Davenport, SL	1
Hefner, MA	1
Mitchell, JA	1
de Chadarévian, JP	1
Kaplan, P	1
Vekemans, M	1
Kaplan, BS	1
Bradley, WG	1
Richardson, J	1
Frew, IJ	1
Mair, IW	1
Pollard, G	1
Neumaier, R	1
Remlein-Mozolewska, G	1
Roberts, SR	1
Mohamed, MA	1
Weiss, DI	1
Ziring, PR	1
Cooper, LZ	1
Schulze, W	1
Ganz, H	1
Oba, N	1
Biéder, J	1
Faidherbe, D	1
Houillon, P	1
Amini-Elihou, S	1
Amin-Zaki, L	1
Wright, VJ	1
Gorlin, RJ	1
Hertzberg, R	1
Ahrendts, H	1

Studies

Magdesian, KG

Williams, DC

Aleman, M

Lecouteur, RA

Madigan, JE

BROBECK, VH

FLEISCHLI, CA

DIGEORGE, AM

OLMSTED, RW

HARLEY, RD

PARTSCH, CJ

HOUGHTON, NI

COUTEAU-LAGARDE, JM

COLLIER, M

PARTINGTON, MW

NATH, K

VIJAY, SD

NEMA, HV

SHUKLA, BR

RUGEL, SJ

KEATES, EU

PAUFIQUE, L

RAVAULT, MP

MORGON, A

ROBINSON, GC

MILLER, JR

SOEPARDEN, LI

POROT, M

FILIU, M

Uyama, S

Aikawa, K

Tomemori, S

Feingold, M

Robinson, MJ

Gellis, SS

Sellars, S

Beighton, P

Donnai, D

Barrow, M

Bassabi, SK

Medji, AP

Doutetien, C

Oussa, G

Hounkpe, YY

Vodouhe, SJ

Babagbeto, M

Latoundji, S

Bard, LA

Hayasaka, S

Noda, S

Setogawa, T

Kobayashi, A

Kishida, K

Sakai, T

Warburg, M

Tommerup, N

Vestermark, S

Parving, A

Weismann, K

Russell, B

Thomsen, HK

Davenport, SL

Hefner, MA

Mitchell, JA

de Chadarévian, JP

Kaplan, P

Vekemans, M

Kaplan, BS

Bradley, WG

Richardson, J

Frew, IJ

Mair, IW

Pollard, G

Neumaier, R

Remlein-Mozolewska, G

Roberts, SR

Mohamed, MA

Weiss, DI

Ziring, PR

Cooper, LZ

Schulze, W

Ganz, H

Oba, N

Biéder, J

Faidherbe, D

Houillon, P

Amini-Elihou, S

Amin-Zaki, L

Wright, VJ

Gorlin, RJ

Hertzberg, R

Ahrendts, H

Reviews

2 reviews available for 2-propanol and Deafness

Article	Year
[A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC]. Journal francais d'ophtalmologie, 1997, Volume: 20, Issue:5 Topics: Benin; Child, Preschool; Deafness; Humans; Iris; Male; Waardenburg Syndrome	1997
Waardenburg syndrome in Japanese patients. Case reports and literature review. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 1992, Volume: 205, Issue:1 Topics: Adult; Albinism, Ocular; Child, Preschool; Deafness; Eye Color; Female; Humans; Incidence; Infant; I	1992

Article

Year

[A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC].

Journal francais d'ophtalmologie, 1997, Volume: 20, Issue:5

Topics: Benin; Child, Preschool; Deafness; Humans; Iris; Male; Waardenburg Syndrome

1997

Waardenburg syndrome in Japanese patients. Case reports and literature review.

Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde, 1992, Volume: 205, Issue:1

Topics: Adult; Albinism, Ocular; Child, Preschool; Deafness; Eye Color; Female; Humans; Incidence; Infant; I

1992

Other Studies

38 other studies available for 2-propanol and Deafness

Article	Year
Evaluation of deafness in American Paint Horses by phenotype, brainstem auditory-evoked responses, and endothelin receptor B genotype. Journal of the American Veterinary Medical Association, 2009, Nov-15, Volume: 235, Issue:10 Topics: Animals; Behavior, Animal; Deafness; Evoked Potentials, Auditory, Brain Stem; Female; Genetic Predis	2009
Cataract, recurrent iritis, and deafness secondary to injury by lightning. American journal of ophthalmology, 1946, Volume: 29 Topics: Cataract; Deafness; Electric Injuries; Electricity; Humans; Inflammation; Iris; Iritis; Lightning	1946
Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects. The Journal of pediatrics, 1960, Volume: 57 Topics: Deafness; Eye Abnormalities; Eyelids; Humans; Iris; Lacrimal Apparatus; Waardenburg Syndrome	1960
[Hereditary deafness in the Waardenburg-Klein syndrome]. Zeitschrift fur Laryngologie, Rhinologie, Otologie und ihre Grenzgebiete, 1962, Volume: 41 Topics: Albinism; Bone Diseases; Deafness; Genetics, Medical; Hearing Loss; Humans; Iris; Nose; Nose Deformi	1962
WAARDENBURG'S SYNDROME WITH DEAFNESS AS THE PRESENTING SYMPTOM. REPORT OF TWO CASES. The New Zealand medical journal, 1964, Volume: 63 Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss;	1964
[THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME]. Journal de genetique humaine, 1963, Volume: 12 Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hair Diseases	1963
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION. Canadian Medical Association journal, 1964, Apr-25, Volume: 90 Topics: Adolescent; Anemia, Iron-Deficiency; Black People; Canada; Child; Deafness; Eye; Eyebrows; Eyelids;	1964
CROUZON'S DISEASE AND PITUITARY DYSFUNCTION. CROUZON'S DISEASE, HYPOPITUITARISM, ECTOPIA LENTIS, SECONDARY GLAUCOMA, AND IRIS ATROPHY IN DEAF-MUTE FAMILY. The British journal of ophthalmology, 1964, Volume: 48 Topics: Adolescent; Atrophy; Craniofacial Dysostosis; Deafness; Ectopia Lentis; Eye Diseases; Genetics, Medi	1964
WAARDENBURG'S SYNDROME IN SIX GENERATIONS OF ONE FAMILY. American journal of diseases of children (1960), 1965, Volume: 109 Topics: Congenital Abnormalities; Deafness; Eyelids; Facial Expression; Genetics, Medical; Hair; Hearing Los	1965
[APROPOS OF THE WAARDENBURG-KLEIN SYNDROME]. Bulletin des societes d'ophtalmologie de France, 1964, Volume: 64 Topics: Child; Deafness; Eye Diseases; Hearing Loss; Humans; Iris; Lacrimal Apparatus; Nose; Nose Deformitie	1964
WAARDENBURG'S SYNDROME: THE RISK OF RECURRENCE OF CONGENITAL DEAFNESS IN A KINDRED. The Journal of pediatrics, 1965, Volume: 67 Topics: Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss; Humans	1965
[A curious syndrome: deaf-mutism, iridal heterochromia and epilepsy]. La Presse medicale, 1959, Oct-03, Volume: 67 Topics: Deafness; Epilepsy; Eye Abnormalities; Humans; Iris; Iris Diseases; Medical Records; Syndrome; Trite	1959
[A second case of deaf-mutism with heterochromia iridis and epilepsy]. Revue d'oto-neuro-ophtalmologie, 1959, Volume: 31 Topics: Deafness; Epilepsy; Humans; Iris; Iris Diseases; Pigmentation Disorders	1959
[Waardenburg's syndrome in three generations of one family]. Nihon ganka kiyo, 1966, Volume: 17, Issue:2 Topics: Adult; Child, Preschool; Chromosomes; Deafness; Female; Humans; Iris; Male; Nose Deformities, Acquir	1966
Waardenburg's syndrome during the first year of life. The Journal of pediatrics, 1967, Volume: 71, Issue:6 Topics: Audiometry; Deafness; Fundus Oculi; Hair; Humans; Infant; Infant, Newborn; Iris; Male; Nose Deformit	1967
The Waardenburg syndrome in deaf children in southern Africa. South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1983, May-07, Volume: 63, Issue:19 Topics: Abnormalities, Multiple; Black or African American; Black People; Color; Deafness; Female; Humans; I	1983
Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder? American journal of medical genetics, 1993, Oct-01, Volume: 47, Issue:5 Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Child, Preschool; Coloboma; Deafness; Female;	1993
Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism. Archives of ophthalmology (Chicago, Ill. : 1960), 1978, Volume: 96, Issue:7 Topics: Abnormalities, Multiple; Adolescent; Adult; Albinism; Child; Child, Preschool; Deafness; Female; Gen	1978
The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndrome. Ophthalmic paediatrics and genetics, 1990, Volume: 11, Issue:3 Topics: Abnormalities, Multiple; Blindness; Child; Coloboma; Cytogenetics; Deafness; Female; Humans; Iris; M	1990
The spectrum of clinical features in CHARGE syndrome. Clinical genetics, 1986, Volume: 29, Issue:4 Topics: Abnormalities, Multiple; Adolescent; Adult; Central Nervous System Diseases; Child, Preschool; Choan	1986
Aniridia/glaucoma and Wilms tumor in a sibship with renal tubular acidosis and sensory nerve deafness. American journal of medical genetics. Supplement, 1987, Volume: 3 Topics: Acidosis, Renal Tubular; Adult; Consanguinity; Deafness; Diabetes Mellitus, Type 1; Genes, Recessive	1987
The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect. Brain : a journal of neurology, 1974, Volume: 97, Issue:3 Topics: Adult; Albinism; Congenital Abnormalities; Corneal Opacity; Deafness; Electromyography; Female; Fund	1974
Hereditary deafness in the white cat. Acta oto-laryngologica. Supplementum, 1973, Volume: 314 Topics: Age Factors; Animals; Cats; Cochlea; Deafness; Ear, Inner; Female; Functional Laterality; Ganglia; G	1973
Vision characteristics of deaf students. American journal of optometry and physiological optics, 1974, Volume: 51, Issue:11 Topics: Adolescent; Adult; Amblyopia; California; Cataract; Child; Child, Preschool; Color Vision Defects; D	1974
[Case of iridoschisis in a 10-year-old girl]. Klinika oczna, 1973, Volume: 43, Issue:2 Topics: Age Factors; Child; Deafness; Eye Diseases; Female; Humans; Iris	1973
Color dilution and hereditary defects in collie dogs. American journal of ophthalmology, 1967, Volume: 63, Issue:6 Topics: Animals; Blindness; Deafness; Dog Diseases; Dogs; Ear; Eye Abnormalities; Fundus Oculi; Genes; Hair;	1967
Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome). Bulletin of the Ophthalmological Society of Egypt, 1971, Volume: 64, Issue:68 Topics: Abnormalities, Multiple; Child; Deafness; Egypt; Eye Abnormalities; Female; Humans; Iris; Osteogenes	1971
Surgery of the rubella cataract. American journal of ophthalmology, 1972, Volume: 73, Issue:3 Topics: Abnormalities, Multiple; Age Factors; Cataract; Cataract Extraction; Child, Preschool; Deafness; Fem	1972
[Hearing disorders in Waardenburg's syndrome]. HNO, 1972, Volume: 20, Issue:7 Topics: Abnormalities, Multiple; Adult; Audiometry; Child; Child, Preschool; Deafness; Eyebrows; Humans; Iri	1972
[A case report of a family of Rieger's anomaly]. Nippon Ganka Gakkai zasshi, 1971, Jan-20, Volume: 75 Topics: Abnormalities, Multiple; Adult; Atropine; Child; Cornea; Deafness; Eye Diseases; Glaucoma; Humans; I	1971
[Heterochromia iridis, hypoacousia and epilepsy in the same family]. Annales medico-psychologiques, 1970, Volume: 1, Issue:1 Topics: Child; Child Behavior Disorders; Deafness; Epilepsy; Humans; Iris; Language Disorders; Male; Pigment	1970
[A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia]. Journal de genetique humaine, 1970, Volume: 18, Issue:4 Topics: Abnormalities, Multiple; Adolescent; Blood Cells; Child; Deafness; Diseases in Twins; Eye Diseases;	1970
An Arab family with Waardenburg syndrome. The Journal of laryngology and otology, 1971, Volume: 85, Issue:5 Topics: Abnormalities, Multiple; Adolescent; Adult; Deafness; Female; Humans; Iraq; Iris; Male; Middle Aged;	1971
Sensorineural hearing loss and congenital heterochromia iridum. Report of a case. American journal of diseases of children (1960), 1968, Volume: 116, Issue:1 Topics: Asian People; Audiometry; Child; Deafness; Ear, External; Humans; Iris; Male; Pigmentation Disorders	1968
Sensorineural hearing loss and congenital heterochromia iridium. American journal of diseases of children (1960), 1969, Volume: 117, Issue:3 Topics: Child; Color; Deafness; Ear; Humans; Iris	1969
Sensorineural hearing loss and congenital heterochromia iridium. American journal of diseases of children (1960), 1969, Volume: 117, Issue:3 Topics: Branchial Region; Child; Color; Deafness; Ear; Humans; Iris	1969
Ocular defects in congenital rubella. The Medical journal of Australia, 1969, Mar-15, Volume: 1, Issue:11 Topics: Atrophy; Cataract; Chorioretinitis; Deafness; Diagnosis, Differential; Edema; Eye Diseases; Female;	1969
[Waardenburg's syndrome demonstrated on 5 families]. Zeitschrift fur Kinderheilkunde, 1965, Sep-03, Volume: 93, Issue:4 Topics: Adolescent; Adult; Child; Deafness; Female; Fundus Oculi; Humans; Iris; Male; Malocclusion; Nose Def	1965

Article

Year

Evaluation of deafness in American Paint Horses by phenotype, brainstem auditory-evoked responses, and endothelin receptor B genotype.

Journal of the American Veterinary Medical Association, 2009, Nov-15, Volume: 235, Issue:10

Topics: Animals; Behavior, Animal; Deafness; Evoked Potentials, Auditory, Brain Stem; Female; Genetic Predis

2009

Cataract, recurrent iritis, and deafness secondary to injury by lightning.

American journal of ophthalmology, 1946, Volume: 29

Topics: Cataract; Deafness; Electric Injuries; Electricity; Humans; Inflammation; Iris; Iritis; Lightning

1946

Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects.

The Journal of pediatrics, 1960, Volume: 57

Topics: Deafness; Eye Abnormalities; Eyelids; Humans; Iris; Lacrimal Apparatus; Waardenburg Syndrome

1960

[Hereditary deafness in the Waardenburg-Klein syndrome].

Zeitschrift fur Laryngologie, Rhinologie, Otologie und ihre Grenzgebiete, 1962, Volume: 41

Topics: Albinism; Bone Diseases; Deafness; Genetics, Medical; Hearing Loss; Humans; Iris; Nose; Nose Deformi

1962

WAARDENBURG'S SYNDROME WITH DEAFNESS AS THE PRESENTING SYMPTOM. REPORT OF TWO CASES.

The New Zealand medical journal, 1964, Volume: 63

Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss;

1964

[THE WHITE FORELOCK AND MYOPIA AS "INDICATOR" FACTORS OF THE WAARDENBURG-KLEIN SYNDROME].

Journal de genetique humaine, 1963, Volume: 12

Topics: Child; Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hair Diseases

1963

WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.

Canadian Medical Association journal, 1964, Apr-25, Volume: 90

Topics: Adolescent; Anemia, Iron-Deficiency; Black People; Canada; Child; Deafness; Eye; Eyebrows; Eyelids;

1964

CROUZON'S DISEASE AND PITUITARY DYSFUNCTION. CROUZON'S DISEASE, HYPOPITUITARISM, ECTOPIA LENTIS, SECONDARY GLAUCOMA, AND IRIS ATROPHY IN DEAF-MUTE FAMILY.

The British journal of ophthalmology, 1964, Volume: 48

Topics: Adolescent; Atrophy; Craniofacial Dysostosis; Deafness; Ectopia Lentis; Eye Diseases; Genetics, Medi

1964

WAARDENBURG'S SYNDROME IN SIX GENERATIONS OF ONE FAMILY.

American journal of diseases of children (1960), 1965, Volume: 109

Topics: Congenital Abnormalities; Deafness; Eyelids; Facial Expression; Genetics, Medical; Hair; Hearing Los

1965

[APROPOS OF THE WAARDENBURG-KLEIN SYNDROME].

Bulletin des societes d'ophtalmologie de France, 1964, Volume: 64

Topics: Child; Deafness; Eye Diseases; Hearing Loss; Humans; Iris; Lacrimal Apparatus; Nose; Nose Deformitie

1964

WAARDENBURG'S SYNDROME: THE RISK OF RECURRENCE OF CONGENITAL DEAFNESS IN A KINDRED.

The Journal of pediatrics, 1965, Volume: 67

Topics: Congenital Abnormalities; Deafness; Eyebrows; Eyelids; Genetics, Medical; Hair; Hearing Loss; Humans

1965

[A curious syndrome: deaf-mutism, iridal heterochromia and epilepsy].

La Presse medicale, 1959, Oct-03, Volume: 67

Topics: Deafness; Epilepsy; Eye Abnormalities; Humans; Iris; Iris Diseases; Medical Records; Syndrome; Trite

1959

[A second case of deaf-mutism with heterochromia iridis and epilepsy].

Revue d'oto-neuro-ophtalmologie, 1959, Volume: 31

Topics: Deafness; Epilepsy; Humans; Iris; Iris Diseases; Pigmentation Disorders

1959

[Waardenburg's syndrome in three generations of one family].

Nihon ganka kiyo, 1966, Volume: 17, Issue:2

Topics: Adult; Child, Preschool; Chromosomes; Deafness; Female; Humans; Iris; Male; Nose Deformities, Acquir

1966

Waardenburg's syndrome during the first year of life.

The Journal of pediatrics, 1967, Volume: 71, Issue:6

Topics: Audiometry; Deafness; Fundus Oculi; Hair; Humans; Infant; Infant, Newborn; Iris; Male; Nose Deformit

1967

The Waardenburg syndrome in deaf children in southern Africa.

South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1983, May-07, Volume: 63, Issue:19

Topics: Abnormalities, Multiple; Black or African American; Black People; Color; Deafness; Female; Humans; I

1983

Diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness: a newly recognized autosomal recessive disorder?

American journal of medical genetics, 1993, Oct-01, Volume: 47, Issue:5

Topics: Abnormalities, Multiple; Agenesis of Corpus Callosum; Child, Preschool; Coloboma; Deafness; Female;

1993

Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism.

Archives of ophthalmology (Chicago, Ill. : 1960), 1978, Volume: 96, Issue:7

Topics: Abnormalities, Multiple; Adolescent; Adult; Albinism; Child; Child, Preschool; Deafness; Female; Gen

1978

The Yemenite deaf-blind hypopigmentation syndrome. A new oculo-dermato-auditory syndrome.

Ophthalmic paediatrics and genetics, 1990, Volume: 11, Issue:3

Topics: Abnormalities, Multiple; Blindness; Child; Coloboma; Cytogenetics; Deafness; Female; Humans; Iris; M

1990

The spectrum of clinical features in CHARGE syndrome.

Clinical genetics, 1986, Volume: 29, Issue:4

Topics: Abnormalities, Multiple; Adolescent; Adult; Central Nervous System Diseases; Child, Preschool; Choan

1986

Aniridia/glaucoma and Wilms tumor in a sibship with renal tubular acidosis and sensory nerve deafness.

American journal of medical genetics. Supplement, 1987, Volume: 3

Topics: Acidosis, Renal Tubular; Adult; Consanguinity; Deafness; Diabetes Mellitus, Type 1; Genes, Recessive

1987

The familial association of neurofibromatosis, peroneal muscular atrophy, congenital deafness, partial albinism, and Axenfeld's defect.

Brain : a journal of neurology, 1974, Volume: 97, Issue:3

Topics: Adult; Albinism; Congenital Abnormalities; Corneal Opacity; Deafness; Electromyography; Female; Fund

1974

Hereditary deafness in the white cat.

Acta oto-laryngologica. Supplementum, 1973, Volume: 314

Topics: Age Factors; Animals; Cats; Cochlea; Deafness; Ear, Inner; Female; Functional Laterality; Ganglia; G

1973

Vision characteristics of deaf students.

American journal of optometry and physiological optics, 1974, Volume: 51, Issue:11

Topics: Adolescent; Adult; Amblyopia; California; Cataract; Child; Child, Preschool; Color Vision Defects; D

1974

[Case of iridoschisis in a 10-year-old girl].

Klinika oczna, 1973, Volume: 43, Issue:2

Topics: Age Factors; Child; Deafness; Eye Diseases; Female; Humans; Iris

1973

Color dilution and hereditary defects in collie dogs.

American journal of ophthalmology, 1967, Volume: 63, Issue:6

Topics: Animals; Blindness; Deafness; Dog Diseases; Dogs; Ear; Eye Abnormalities; Fundus Oculi; Genes; Hair;

1967

Inter-oculo-irido-auditory dysplasia. (Waardenburg, van der Hoeve, Halberstsma syndrome).

Bulletin of the Ophthalmological Society of Egypt, 1971, Volume: 64, Issue:68

Topics: Abnormalities, Multiple; Child; Deafness; Egypt; Eye Abnormalities; Female; Humans; Iris; Osteogenes

1971

Surgery of the rubella cataract.

American journal of ophthalmology, 1972, Volume: 73, Issue:3

Topics: Abnormalities, Multiple; Age Factors; Cataract; Cataract Extraction; Child, Preschool; Deafness; Fem

1972

[Hearing disorders in Waardenburg's syndrome].

HNO, 1972, Volume: 20, Issue:7

Topics: Abnormalities, Multiple; Adult; Audiometry; Child; Child, Preschool; Deafness; Eyebrows; Humans; Iri

1972

[A case report of a family of Rieger's anomaly].

Nippon Ganka Gakkai zasshi, 1971, Jan-20, Volume: 75

Topics: Abnormalities, Multiple; Adult; Atropine; Child; Cornea; Deafness; Eye Diseases; Glaucoma; Humans; I

1971

[Heterochromia iridis, hypoacousia and epilepsy in the same family].

Annales medico-psychologiques, 1970, Volume: 1, Issue:1

Topics: Child; Child Behavior Disorders; Deafness; Epilepsy; Humans; Iris; Language Disorders; Male; Pigment

1970

[A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].

Journal de genetique humaine, 1970, Volume: 18, Issue:4

Topics: Abnormalities, Multiple; Adolescent; Blood Cells; Child; Deafness; Diseases in Twins; Eye Diseases;

1970

An Arab family with Waardenburg syndrome.

The Journal of laryngology and otology, 1971, Volume: 85, Issue:5

Topics: Abnormalities, Multiple; Adolescent; Adult; Deafness; Female; Humans; Iraq; Iris; Male; Middle Aged;

1971

Sensorineural hearing loss and congenital heterochromia iridum. Report of a case.

American journal of diseases of children (1960), 1968, Volume: 116, Issue:1

Topics: Asian People; Audiometry; Child; Deafness; Ear, External; Humans; Iris; Male; Pigmentation Disorders

1968

Sensorineural hearing loss and congenital heterochromia iridium.

American journal of diseases of children (1960), 1969, Volume: 117, Issue:3

Topics: Child; Color; Deafness; Ear; Humans; Iris

1969

Sensorineural hearing loss and congenital heterochromia iridium.

American journal of diseases of children (1960), 1969, Volume: 117, Issue:3

Topics: Branchial Region; Child; Color; Deafness; Ear; Humans; Iris

1969

Ocular defects in congenital rubella.

The Medical journal of Australia, 1969, Mar-15, Volume: 1, Issue:11

Topics: Atrophy; Cataract; Chorioretinitis; Deafness; Diagnosis, Differential; Edema; Eye Diseases; Female;

1969

[Waardenburg's syndrome demonstrated on 5 families].

Zeitschrift fur Kinderheilkunde, 1965, Sep-03, Volume: 93, Issue:4

Topics: Adolescent; Adult; Child; Deafness; Female; Fundus Oculi; Humans; Iris; Male; Malocclusion; Nose Def

1965