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Kabuki make-up syndrome with genitourinary anomalies, ophthalmologic features and hyperpigmentation in an Egyptian child
Egyptian Journal of Medical Human Genetics [The]. 2017; 18 (1): 87-92
Dans Anglais | IMEMR | ID: emr-189222
ABSTRACT
We report a 3.5 year old male child, first in order of birth of healthy consanguineous Egyptian parents with typical characteristics of Kabuki make-up syndrome. The patient had microcephaly, high arched sparse eyebrows, hypertelorism, long palpebral fissures with eversion of the lateral third of the lower eyelids, bilateral ptosis, long eyelashes, blue sclera, depressed nasal bridge, broad nose with everted nares, and low set small deformed ears, thin lips, low post hair line, short neck, persistent fingertip pads, dysplastic nails, hypermobile joints, pigmented nevus on the back, lateral side of right foot and right leg and mild hypertrichosis over the lower back. Our patient had also a non-functioning left kidney, multiple chalazions in upper eyelids, enlargement of the glans penis, which were not reported previously, and moderate mental retardation
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Indice: Méditerranée orientale Sujet Principal: Malformations urogénitales / Maladies vestibulaires / Enfant / Hyperpigmentation / Oeil / Face / Hémopathies / Déficience intellectuelle Type d'étude: Enquête cas-témoins / Études cas/témoins Limites du sujet: Enfant d'âge préscolaire / Humains / Mâle langue: Anglais Texte intégral: Egypt. J. Med. Hum. Genet. Année: 2017

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Recherche sur Google
Indice: Méditerranée orientale Sujet Principal: Malformations urogénitales / Maladies vestibulaires / Enfant / Hyperpigmentation / Oeil / Face / Hémopathies / Déficience intellectuelle Type d'étude: Enquête cas-témoins / Études cas/témoins Limites du sujet: Enfant d'âge préscolaire / Humains / Mâle langue: Anglais Texte intégral: Egypt. J. Med. Hum. Genet. Année: 2017