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PubMed journal article [INCONTINENTIA ALVI were found in PRIME PubMed. Download Prime PubMed App to iPhone or iPad. PubMed journal article [Sphincteroplasty in incontinentia alvi were found in PRIME PubMed. Download Prime PubMed App to iPhone or iPad. Author: KUMMER A, Journal: Nederlands tijdschrift voor geneeskunde[/11].

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In addition, the Dictionary is now supplemented with millions of real-life translation examples from external sources. Alport syndrome Dent’s disease X-linked nephrogenic diabetes insipidus. Suggest a new entry. Pigmentation disordersTemplate: It is not inherited and does not involve skin stages 1 or 2.

Incontinentia pigmenti

Show summary of all matches incontinentia. The TJEM also covers the fields of disaster-prevention science, including earthquake archeology. Genetic counselingprenatal testing, and preimplantation genetic diagnosis is available. Color blindness red and green, but not blue Ocular albinism 1 Norrie disease Choroideremia Other: By using this site, you agree to the Terms incobtinentia Use and Privacy Policy.

X-linked dominant inheritance works differently depending upon whether the mother left image or father right image is the carrier of a gene that causes a disease or disorder.


DNA replication and repair-deficiency disorder. An error has occured. Journal home Journal issue Featured articles About the journal.

Concerning blood picture, Hiro 12 stated that there was no remarkable difference from normal blood picture, but that the nuclei of neutrophiles shifted more or less to the left. Albi Waardenburg syndrome Tietz syndrome.


It is named from its appearance under a microscope. Vasospastic macule Woronoff’s ring Nevus anemicus. November 28, accepted: Most newborns with IP will develop discolored skin within the first two weeks. The main sources we used are professionally translated company, and academic, websites. My own case of Hirschsprung’s disease was accompanied with encopresis too. Not to be confused with Incontinentia pigmenti achromians.

In my own case it was very remarkable, for the cells with O-typed nucleus appeared in the highest percentage among the staff cells.

Costello syndrome Kindler syndrome Laryngoonychocutaneous syndrome Skin fragility syndrome. The editorially approved PONS Online Dictionary with text translation tool now includes a database with hundreds of millions of real translations from the Internet. Such testing is available clinically. Are you missing a word, phrase or translation? Aovi sign in or register for free if you want to use this function.

Incontinentia pigmenti – Wikipedia

Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly of the flexures Naegeli—Franceschetti—Jadassohn syndrome Dyskeratosis congenita X-linked reticulate pigmentary disorder Galli—Galli disease Revesz syndrome. Neurological problems can include: Javascript has been deactivated in incnotinentia browser. The PONS Dictionary delivers the reliability of a dictionary which has been editorially reviewed and expanded over the course of decades.

Your message has now been forwarded to the PONS editorial department. Capillary hemangioma Port-wine stain Nevus flammeus nuchae. Shirono 5 reported one case of Hirschsprung’s disease in cases incontlnentia encopresis, and he stated that it was a question whether incontinentia alvi was a symptom of Hirschsprung’s disease or Hirschsprung’s disease was accompanied with encopre sis.


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A Case of Megalosigmoid with Incontinentia Alvi; and the Nuclear Picture

Dyskeratosis congenita Hypohidrotic ectodermal dysplasia EDA X-linked ichthyosis X-linked endothelial corneal dystrophy. We are working on continually optimizing the quality of our usage examples by improving their relevance as well as the translations.

So, now you can see how a concept is translated in specific contexts. Please do leave them untouched.

Neurofibromatosis type I Watson syndrome Tuberous sclerosis. Acanthosis nigricans Incontinenti Familial progressive hyperpigmentation Pallister—Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis.

IP is ali in an X-linked dominant manner. In females, the cells expressing the mutated IKBKG gene due to lyonization selectively die around the time of birth so the X-inactivation is extremely skewed. Retrieved 26 December Carotenosis Tattoo Tar melanosis.