Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Newborn transient patterned hyperpigmentation and anophthalmia.

Boletin medico del Hospital Infantil de Mexico - 1 Jan 2020

Chacón Camacho Oscar F, Arce-González Rocío, Rodríguez Uribe Genaro

Abstract excerpt

Background: Transient pigmentary lines of the newborn are uncommon cutaneous lesions of unknown etiology. To date, only a few cases have been described. Case report: A patient with a combination of transient pigmentary lines and ocular malformation is described. Molecular analysis of the SRY-box 2 (SOX2) and MIFT genes was conducted to rule out any monogenetic etiology. Conclusions: Worldwide, this is the eighth...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anophthalmos
Share to Hyperpigmentation
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Source

Identifiers

PMID: 32496470
DOI: 10.24875/BMHIM.19000191

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Newborn transient patterned hyperpigmentation and anophthalmia.PMID 32496470Read ↗

Clinical Features of Postnatal Pigmented Macular Lesions on the Pediatric Facial RegionSemantic proximity Read ↗

Delineation of a newly recognized neurocutaneous malformation syndrome with "cutis tricolor".Semantic proximity Read ↗

A novel pathogenic RHOA variant in a patient with patterned cutaneous hypopigmentation associated with extracutaneous findings.Semantic proximity Read ↗

Cutis tricolor: congenital hyper- and hypopigmented lesions in a background of normal skin with and without associated systemic features: further expansion of the phenotype.Semantic proximity Read ↗

Congenital linear streaks on the face and neck and microphthalmia in an infant girl.Semantic proximity Read ↗

Recurrent Vascularizing Keratitis in Infants With Hereditary Mucoepithelial Dysplasia Related to SREBF1 Mutation.Semantic proximity Read ↗

Generalized mottled pigmentation with postnatal skin blistering in three generations.Semantic proximity Read ↗

Bullous lesions following phototherapy in a newborn.Semantic proximity Read ↗

Hyperpigmented Spots at Fundus Examination: A New Ocular Sign in Neurofibromatosis Type ISemantic proximity Read ↗

"Cutis tricolor": congenital hyper- and hypopigmented macules associated with a sporadic multisystem birth defect: an unusual example of twin spotting?Semantic proximity Read ↗

Patterned hypopigmentation associated with prenatally diagnosed trisomy 7 mosaicism: long-term follow-up.Semantic proximity Read ↗

Hereditary congenital hypopigmented and hyperpigmented macules (Westerhof syndrome) in two siblingsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.