Edit concept Question Editor Create issue ticket

Ectodermal Dysplasia Type Tricho-Odonto-Onychial


Presentation

  • A review of seventeen ectodermal dysplasias is presented for different diagnosis.[ncbi.nlm.nih.gov]
  • A review of seventeen ectodermal dysplasias is presented for differential diagnosis.[onlinelibrary.wiley.com]
  • The eldest affected sister also presents fronto- parietal skull deficiency similar to that of the proposita.[docslide.net]
  • The information presented is not intended to replace medical advice or treatment from your own doctor or healthcare provider.[wellnessadvocate.com]
Nail Abnormality
  • Ackerman et al. [19731 de- scribed 3 sibs with scalp hypotrichosis, deafness, finger syndactyly 3-4, and skin and nail abnormalities, but they had glaucoma and coarse, stiff hand skin.[documents.tips]
Enuresis
  • Engelhard–Yatziv syndrome Englemann disease Enolase deficiency type 1 Enolase deficiency type 2 Enolase deficiency type 3 Enolase deficiency type 4 Enolase deficiency Enterobiasis Enteropathica Enterovirus antenatal infection Entomophthoramycosis Enu–Env Enuresis[wikiwand.com]
Widely Spaced Teeth
  • spaced teeth and hypoplastic enamel; sparse cafe-au-lait spots on back; irregular outlines of areolae; right nipple with hypertrophied Montgomery glands; supernumerary left nipple; mild palmoplantar keratosis; bilateral syndactyly of toes 2 and 3; discrete[docslide.us]
Microdontia
  • […] hair at the occipital and temporal regions; blond, scant eyebrows and lashes; absent axillary and pubic hair; fragile and brittle fingernails with a subungual corneal layer; thick and brittle toenails also with a subungual corneal layer; hypodontia, microdontia[docslide.us]
Esotropia
  • Normal findings: similar to those of her sister; no esotropia was verified. The patient was married and had a pregnancy that ended in a spontaneous abortion.[docslide.us]
  • Erythropoietic protoporphyria Es-Et Escher Hirt syndrome Esophageal atresia associated anomalies Esophageal atresia coloboma talipes Esophageal atresia Esophageal disorder Esophageal duodenal atresia abnormalities of hands Esophageal neoplasm Esophageal varices Esotropia[wikidoc.org]
  • Erythropoietic protoporphyria Escher Hirt syndrome Esophageal atresia associated anomalies Esophageal atresia coloboma talipes Esophageal atresia Esophageal disorder Esophageal duodenal atresia abnormalities of hands Esophageal neoplasm Esophageal varices Esotropia[bioreference.net]
  • […] syndrome Escherichia coli infection Esophageal atresia associated anomalies Esophageal atresia coloboma talipes Esophageal atresia Esophageal disorder Esophageal duodenal atresia abnormalities of hands Esophageal neoplasm Esophageal varices Esophoria Esotropia[wikiwand.com]
  • Esotropia Essential hypertension[?] Essential iris atrophy[?] Essential mixed cryoglobulinemia[?] Essential thrombocytopenia[?] Essential thrombocytosis[?] Esthesioneuroblastoma[?] Ethylmalonic aciduria[?] Ethylmalonic adipic aciduria[?][encyclopedia.kids.net.au]
Sparse Hair
  • hair * Sparse eyelashes * Sparse eyebrows * Freckles Causes - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
  • In some types, teeth may be missing and nails may be defective, while in another type there may be missing teeth, inability to sweat, and sparse hair. Still another may have hearing loss and defects of the enamel of the teeth.[nfed.org]
  • hair-short stature-skin anomalies syndrome Superficial epidermolytic ichthyosis Suprabasal epidermolysis bullosa simplex Syndromic hair shaft abnormality Syndromic recessive X-linked ichthyosis Taurodontia-absent teeth-sparse hair syndrome Teebi-Shaltout[se-atlas.de]
  • Signs & Symptoms HED is characterized by lack of or diminished sweating (anhidrosis or hypohidrosis), abnormally sparse hair (hypotrichosis), and/or absence (hypodontia) and/or malformation of certain teeth.[rarediseases.org]
  • Winter RM, MacDermot KD, Hill FG (1988): Sparse hair, short stature, hypoplastic thumbs, single upper central incisor and ab- normal skin pigmentation: a possible new form of ectodermal dysplasia. Am J Med Genet 29:209-216.[documents.tips]
Sparse Eyebrows
  • eyebrows * Freckles Causes - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
  • Patients with Zlotogora-Ogur syndrome [Rodini and Richieri-Costa, 19901 are mentally retarded, with hypo- trichosis, laterally sparse eyebrows, finger syndactyly 2-4 and toe syndactyly 2-3/34, hypohidrosis, dry skin, and nail dystrophy.[documents.tips]
Sparse Eyelashes
  • eyelashes * Sparse eyebrows * Freckles Causes - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
Sparse to No Eyebrows
  • […] eyelashes * Sparse eyebrows * Freckles Causes - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
Freckles
  • […] onychial type * Reduced hair growth * Missing teeth * Irregular pigmentation on back * Absent breasts * Mild nerve hearing loss * Under developed nipples * Absent nipples * Abnormal nails * Thick nails * Sparse hair * Sparse eyelashes * Sparse eyebrows * Freckles[checkorphan.org]
Mental Deterioration
  • […] pretibial Epidermolysis bullosa Epidermolytic hyperkeratosis Epidermolytic palmoplantar keratoderma Vorner type Epidi Epididymitis Epil-Epis Epilepsy benign neonatal dominant form Epilepsy benign neonatal recessive form Epilepsy juvenile absence Epilepsy mental[wikidoc.org]
  • deterioration Finnish type Epilepsy microcephaly skeletal dysplasia Epilepsy occipital calcifications Epilepsy progressive myoclonic type 2 Epilepsy telangiectasia Epilepsy with myoclono-astatic crisis Epilepsy, benign occipital Epilepsy, myoclonic progressive[bioreference.net]
  • deterioration Finnish type Epilepsy microcephaly skeletal dysplasia Epilepsy occipital calcifications Epilepsy progressive myoclonic Epilepsy telangiectasia Epilepsy with myoclono-astatic crisis Epilepsy, benign occipital Epilepsy, myoclonic progressive[wikiwand.com]
  • Epilepsy mental deterioration Finnish type[?] Epilepsy microcephaly skeletal dysplasia[?] Epilepsy occipital calcifications[?] Epilepsy progressive myoclonic type 2[?] Epilepsy telangiectasia[?] Epilepsy with myoclono-astatic crisis[?][encyclopedia.kids.net.au]

Treatment

  • Stay at the forefront of your field with updated treatment methods throughout, as well as an increased focus on patients with skin of color.[books.google.de]
  • Treatment - Ectodermal dysplasia tricho odonto onychial type Not supplied. Resources - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
  • The information presented is not intended to replace medical advice or treatment from your own doctor or healthcare provider.[wellnessadvocate.com]
  • The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.[orpha.net]
  • The ad- vent of so many unusual antidepressants has pro- vided diverse more opportunities for prosperous treatment (see Pharmacology Corner).[astakask.com]

Prognosis

  • Prognosis - Ectodermal dysplasia tricho odonto onychial type Not supplied. Treatment - Ectodermal dysplasia tricho odonto onychial type Not supplied. Resources - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
  • A second line category of medications used to treat PD are the monoamine oxidase (a chemical that assists in Prognosis storing certain chemicals in nerve cells) inhibitors (MAOI).[allstatecapital.com]

Etiology

  • Etiology SSPS is due to homozygous or compound heterozygous mutations in WNT10A. Incomplete/localized disease expression in heterozygous carriers and multiple instances of consanguinity occasionally lead to a pseudodominant transmission.[orpha.net]
  • GREENSEEK Fee required for full report. » Virtual Children s Hospital enchondromatosis Clinical presentation, etiology and imaging findings. 75.[www4.geometry.net]

Epidemiology

  • Summary Epidemiology More than 25 cases with SSPS have been described so far. Clinical description SSPS refers to a discrete phenotype of ectodermal dysplasia with a relatively benign course and late diagnosis, often established in adulthood.[orpha.net]
  • A Clinical, Genetic and Epidemiological Study. Baltimore : Johns Hopkins Press. Goodman, R.M., Gorlin, R.J. 1970. The Face in Genetic Disorders. Saint Louis : The C.V. Mosby Co. Gorlin, R.J., Pindborg, J.J. 1964. Syndromes of the Head and Neck.[cambridge.org]
Sex distribution
Age distribution

Prevention

  • Prevention - Ectodermal dysplasia tricho odonto onychial type Not supplied.[checkorphan.org]
  • And are not intended to diagnose, treat, cure or prevent disease. The information presented is not intended to replace medical advice or treatment from your own doctor or healthcare provider.[wellnessadvocate.com]
  • Secondly, the comprehension of the biological mechanisms that cause EDs is needed for the design of efficient prevention and treatment approaches. 2009 Wiley‐Liss, Inc.[scipers.com]
  • Physicians may recommend that impacted nasal secretions be carefully removed on a regular basis to help prevent or limit the severity of rhinitis.[rarediseases.org]
  • Your skin Holds body fluids in, preventing dehydration Keeps harmful microbes out, preventing infections Helps you feel things like heat, cold, and pain Keeps your body temperature even Makes vitamin D when the sun shines on it Anything that irritates[icdlist.com]

Ask Question

5000 Characters left Format the text using: # Heading, **bold**, _italic_. HTML code is not allowed.
By publishing this question you agree to the TOS and Privacy policy.
• Use a precise title for your question.
• Ask a specific question and provide age, sex, symptoms, type and duration of treatment.
• Respect your own and other people's privacy, never post full names or contact information.
• Inappropriate questions will be deleted.
• In urgent cases contact a physician, visit a hospital or call an emergency service!