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Dental agenesis in Kallmann syndrome individuals with FGFR1 mutations

✍ Scribed by ISABELLE BAILLEUL-FORESTIER; CATHERINE GROS; DELPHINE ZENATY; SÉLIM BENNACEUR; JULIANE LEGER; NICOLAS De ROUX

Book ID
108829568
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
176 KB
Volume
20
Category
Article
ISSN
0960-7439

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Kallmann syndrome: 14 novel mutations in
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)
✍ Juliette Albuisson; Chistophe Pêcheux; Jean-Claude Carel; Didier Lacombe; Bruno 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 421 KB

## Kallmann syndrome (KAL) combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is due to Gonadotropin Releasing Hormone (GnRH) deficiency and anosmia is related to hypoplasia of the olfactory bulbs. Occasional symptoms include renal agenesis, bimanual synkinesia, cleft lip palate, dent