Results 71 to 80 of about 434,230 (174)

A Rare Case of Cutaneous Extramedullary Hematopoiesis in Chronic Myeloid Leukemia

Journal of Cutaneous Pathology, Volume 53, Issue 9, Page 767-771, September 2026.
ABSTRACT Cutaneous extramedullary hematopoiesis (CEH) is a rare manifestation of extramedullary hematopoiesis (EMH), a process typically associated with fetal development or myeloproliferative neoplasms. EMH most commonly involves the spleen, liver, and lymph nodes, with CEH being exceedingly rare in chronic myeloid leukemia (CML).
Bennett Christie‐Nguyen, Hanadi El Achi, Levani Iashvili, Amer Wahed, Brenda Mai, Jacob Armstrong   +5 more
wiley   +1 more source

Two Paralogues as They Like It: Conserved and Divergent Evolution of Vertebrate Gcm Genes

Evolution &Development, Volume 28, Issue 3, September 2026.
Comparative overview of Gcm1 and Gcm2 paralogues across vertebrates. Gcm2 is conserved in pharyngeal‐derived organs across gnathostomes, whereas Gcm1 shows lineage‐specific diversification from an ancestral pharyngeal context, including secondary loss in teleosts, distinct expression in bichir gills and skin, and broader expression in mammals ...
Takanori Shono, Norifumi Tatsumi, Tsutomu Miyake, Shigehiro Kuraku, Masataka Okabe   +4 more
wiley   +1 more source

Prenatal diagnosis of focal dermal hypoplasia: Report of three fetuses and review of the literature [PDF]

, 2017
Focal dermal hypoplasia (FDH) is a rare syndrome characterized by pleiotropic features knowing to involve mostly skin and limbs. Although FDH has been described in children and adults, the cardinal signs of the fetal phenotype are not straightforward ...
Triau, Stéphane, A.L. Delezoide, Scheidecker, Sophie, Colin, Estelle, M.P. Lombardi, Kohler, Monique, L. Mary, Antal, Maria Cristina, S. Triau, K.H. Grzeschik, Lombardi, Maria-Paola, E. Colin, M. Gérard, S. Scheidecker, Delezoide, Anne-Lise, Auberger, Elisabeth, M. Kohler, Mary, Laura, Grzeschik, Karl-Heinz, H. Dollfus, M.Cristina Antal, E. Auberger, Dollfus, Hélène, Gérard, Marion   +23 more
core   +1 more source

Expert Treatment Considerations for Lower Face and Neck Rejuvenation

Dermatological Reviews, Volume 7, Issue 4, August 2026.
ABSTRACT Background The lower face and neck are essential to overall facial harmony and a balanced appearance. Although most nonsurgical treatments have focused on the upper and midface, a variety of minimally invasive options are now available for treating the lower face and neck that target different aesthetic concerns and provide welcome ...
Sabrina Fabi, John Fezza, Jeremy B. Green, Jean Carruthers, Nazanin Ashourian, Elena Dimitrijevic, Steven Yoelin   +6 more
wiley   +1 more source

An Unexpected Airway Complication in a Male Patient with Goltz Syndrome

Case Reports in Anesthesiology, 2016
Goltz syndrome, also known as focal dermal hypoplasia, is a rare X-linked dominant multisystem syndrome presenting with cutaneous, skeletal, dental ocular, central nervous system and soft tissue abnormalities.
Sadie Smith, Kavita Gadhok, Dmitri Guvakov   +2 more
doaj   +1 more source

Lymphatic Endothelial Cells in Health and Disease

MedComm, Volume 7, Issue 8, August 2026.
Lymphatic endothelial cells (LECs) are dynamic regulators of tissue homeostasis and disease remodeling. In the healthy state, LECs coordinate interstitial fluid drainage, intestinal lipid transport, and immune trafficking and tolerance. Across disease settings, however, these same programs become maladaptively reprogrammed, contributing to barrier ...
Du Tang, Wang Lin, Hengyang Liu, Jixin Zhong, Shiliang Li, Xiaoquan Rao   +5 more
wiley   +1 more source

Focal dermal hypoplasia: a case report and literature review

, 2011
Focal dermal hypoplasia (FDH), also known as Goltz-Gorlin syndrome, is an autosomal dominant disease affecting tissues derived from the ectoderm and mesoderm.
Lira Ortega, Adriana de Oliveira, Guimaraes, Antonio Sergio [UNIFESP], Goncalves-Bittar, Daniela, Murakami, Christiana, Ana Lídia Ciamponi, Antônio Sérgio Guimarães, Marcelo Bönecker, Christiana Murakami, Boenecker, Marcelo, Ciamponi, Ana Lidia, Daniela Gonçalves-Bittar, Adriana de Oliveira Lira Ortega   +11 more
core   +1 more source

Focal dermal hypoplasia in a male patient due to mosaicism for a novel PORCN single nucleotide deletion

, 2011
Background Focal dermal hypoplasia (FDH) is an X-linked dominant disorder caused by nonsense mutations and deletions in the PORCN gene coding for a transmembrane endoplasmic reticulum protein required for Wingless signalling.
van den Heuij, L. G. T., Steijlen, P. M., van Steensel, M. A. M., van Geel, M., Vreeburg, M.   +4 more
core   +1 more source

Tonsillar Hypertrophy in Goltz-Gorlin Syndrome: Case Report and Literature Review

B-ENT, 2023
Goltz-Gorlin syndrome, also known as focal dermal hypoplasia or nevoid basal cell carcinoma syndrome, is a rare multisystemic disease caused by autosomal dominant mutations in the PORCN gene.
Emilie Lavrysen, Bart Loeys, Olivier M. Vanderveken, An Boudewyns   +3 more
doaj   +2 more sources

DETECTING PORCN MICRODELETIONS IN A LARGE FAMILY WITH FOCAL DERMAL HYPOPLASIA

, 2015
Detecting PORCN microdeletions in a large family with focal dermal hypoplasia: Focal dermal hypoplasia (FDH), an X-linked dominant disease with a highly variable phenotype, presents mainly with congenital linear pigmentation of the skin, herniation of ...
Seven, M., Bozoglu, T. M., Tolun, A., Guven, A.   +3 more
core   +1 more source